Publications

Publications and Patents

2024

256.	J. Kumar, S. Manna, L. J Gooßen, Org. Lett., 2024: Introduction of the Trifluoropropionate Moiety into Aromatic Rings via Rhodium-Catalyzed Coupling of Arylboronic Acids with Diazoesters


255.	B. Xue, F. Papp, M. Yang, J. Shen, A. Doppiu, L. J Gooßen, ACS Catal., 2024, 14, 15, 11172–11177: Pd-Methylnaphthyl-^tBuBrettPhos Complexes as Efficient and Selective Catalysts for the Monoarylation of Ammonia and Hydrazine

254.	J. F. Goebel, J. Stemmer, N. Krüger, N. Sakhaee, L. J Gooßen, Angew. Chem. Int. Ed., 2024, e202408974: Coupling of Aryl Chlorides with Lithium Nucleophiles Enabled by Molecularly Defined Alkynyllithium Palladium Catalysts

253.	M. Hassler, G. Heinrich, M. Kondratiuk, L. J Gooßen, Patent WO 2024088964A1, 2024: Method for producing polyfluorinated tertiary alcohols

252.	J. F. Goebel, F. Belitz, D. Sowa Prendes, Y. Haver, P. Diehl, M. Muhler, L. J Goossen, ChemSusChem, 2024, 17, 14, e202400094: Decarboxylative Ketonization of Aliphatic Carboxylic Acids in a Continuous Flow Reactor Catalysed by Manganese Oxide on Silica

251.	G. Heinrich, M. Kondratiuk, L. J. Gooßen, M. P. Wiesenfeldt, Nat Protoc, 2024, 19, 1529–1556: Rapid reaction optimization by robust and economical quantitative benchtop ¹⁹F NMR spectroscopy

250.	P. J. Kohlpaintner, N. Schupp, N. Ehlenz, L. Marquart, L. J. Gooßen, S. R. Waldvogel, Org. Lett., 2024, 26, 8, 1607–1611: Synthesis of Aromatic N-Oxides Using Electrochemically Generated Peroxodicarbonate

249.	F. Sprang, N. Schupp, P. Kohlpaintner, L. J. Gooßen, S. R. Waldvogel, Green Chem., 2024, 26, 5862–5868: E-Dakin Reaction: Oxidation of Hydroxybenzaldehydes to Phenols with Electrochemically Generated Peroxodicarbonate as Sustainable Ex-Cell Oxidizer

248.	S. A. Varenichenko, V. Markov, J. F. Goebel, O. K. Farat, L. J. Gooßen, J. Org. Chem., 2024, 89, 5, 2840–2846: Vilsmeier−Haack-Initiated Formylative Rearrangement of Spirodioxo-lan-5-ones into Functionalized 4,5,6,7-Tetrahydrobenzofurans

247.	S. Manna, F. Papp, Y. Hisata, J. Löffler, M. Rybka, V. Däschlein-Gessner, Y. Hoshimoto, L. J. Goossen, Adv. Synth. Catal., 2024, 366, 5, 1107–1112: Palladium-Catalyzed γ-Arylation of Acylketene Synthons with Aryl Chlorides Enabled by Ylide-Functionalized Phosphines (YPhos)

2023

246.	Luo, Z. Li, Y. Zheng, Y. Lin, H. Jiang, L. J. Gooßen, M. Lei, L. Huang, ACS Catal., 2023, 13, 18, 12104–12113: Ligand-Enabled ortho-Arylation of (hetero)Aromatic Acids with 2,6-Disubstituted Aryl Halides

245.	D. Sowa Prendes, F. Papp, N. Sankaran, N. Sivendran, F. Beyer, C. Merten, L. J. Gooßen, Angew. Chem. Int. Ed., 2023, e202309868: Enantioselective Synthesis of Arylglycines via Pd-Catalyzed Coupling of Schöllkopf Bis-Lactim Ethers with Aryl Chlorides

244.	B. Xue, J. Shen, S. Manna, A. Doppiu, L. J. Gooßen, Adv. Synth. Catal., 10.1002/adsc.202300761: Selective Monoarylation of Ammonium Triflate with Aryl Chlorides Catalyzed by [Pd(β-MeNAP)Br]₂ and AdBrettPhos

243.	T. van Lingen, V. Bragoni, M. Dyga, B. Exner, D. Schick, C. Held, G. Sadowski, L. J. Gooßen, Angew. Chem. Int. Ed., 2023, 62, e202210009: Carboxylation of Acetylene without Salt Waste: Green Synthesis of C₄ Chemicals Enabled by a CO₂-Pressure Induced Acidity Switch

242.	F. Papp, D. Sowa Prendes, S. Manna, A.-K. Seitz, S. Kostiukovska, J. Löffler, V. H. Gessner, L. J. Gooßen, ACS Catal., 2023, 13, 6846–6850: Palladium-Catalyzed Arylation of Hydantoins with Aryl Chlorides Enabled by Ylide-Functionalized Phosphines (YPhos)

241.	P. J. Kohlpaintner, L. Marquart, L. J. Gooßen, S. R. Waldvogel, Eur. J. Org. Chem., 2023, e202300220: The Oxidation of Organo‐Boron Compounds Using Electrochemically Generated Peroxodicarbonate

240.	M. Kondratiuk, D. Gopinath, A. Elrrays, L. J. Gooßen, Eur. J. Lipid Sci. Technol., 2023, 125, 2200163: Double-Bond Isomerization of Rapeseed Oil Methyl Esters in a Continuous Flow Reactor Efficiently Catalyzed by H-Mordenite

239.	J. F. Goebel, J. Löffler, Z. Zeng, J. Handelmann, A. Hermann, I. Rodstein, T. Gensch, V. H. Gessner, L. J. Goossen, Angew. Chem. Int. Ed., 2023, 62, e202216160: Computer-Driven Development of Ylide Functionalized Phosphines for Palladium-Catalyzed Hiyama Couplings

238.	G. Bertoli, Á. M. Martínez, J. F. Goebel, D. Belmonte, N. Sivendran, L. J. Gooßen, Angew. Chem. Int. Ed., 2023, 62, e202215920: C−H Fluoromethoxylation of Arenes by Photoredox Catalysis

237.	J. F. Goebel, J. Stemmer, F. Belitz, L. J. Goossen, Angew. Chem. Int. Ed., 2023, e202301839: Manganese(I) Catalyzed ortho C–H Allylation of Benzoic Acids

2022

236.	D. Lichte, N. Pirkl, G. Heinrich, S. Dutta, J. F. Goebel, D. Koley, L. J. Gooßen, Angew. Chem. Int. Ed., 2022, e202210009: Palladium-Catalyzed para-C−H Arylation of Anilines with Aromatic Halides

235.	X.-J. Wei, B. Xue, J. Handelmann, Z. Hou, H. Dermandeh, V. H. Gessner, L. J. Goossen, Adv. Synt. Catal., 2022, 364, 19, 3336–3341: Ylide-Functionalized Diisopropyl Phosphine (prYPhos): A Ligand for Selective Suzuki-Miyaura Couplings of Aryl Chlorides

234.	A.K. Seitz, T. van Lingen, M. Dyga, P. J. Kohlpaintner, S. R. Waldvogel, L. J. Goossen, Synlett., 2022, 33, 15, 1527-1531: Amine Oxidation by Electrochemically Generated Peroxodicarbonate

233.	F. Belitz, A.-K. Seitz, J. F. Goebel, Z. Hu, L. J. Goossen, Org. Lett., 2022, 24, 19, 3466–3470: Ru-Catalyzed C–H Arylation of Acrylic Acids with Aryl Bromides

232.	A.-K. Seitz, P. J. Kohlpaintner, T. van Lingen, M. Dyga, F. Sprang, M. Zirbes, S. R. Waldvogel, L. J. Goossen, Angew. Chem. Int. Ed., 2022, 61, e202117563: Concentrated Aqueous Peroxodicarbonate: Efficient Electrosynthesis and Use as Oxidizer in Epoxidations, S-, and N-Oxidations

231.	N. Sivendran, F. Belitz, D. Sowa Prendes, Á. M. Martínez, R. Schmid, L. J. Goossen, Chem. Eur. J., 2022, 28, e2021036: Photochemical Sandmeyer-type Halogenation of Arenediazonium Salts

230.	J. F. Goebel, Z. Zeng, L. J. Gooßen, Synthesis, 2022, 54, 565-569: Biaryl Synthesis via Electrooxidative Transition Metal Catalyzed C−H Activation

2021

229.	T. Haas, C. Richter, L. J. Gooßen, J. F. Goebel, F. Belitz, M. Beller, R. Razzaq, R. Jackstell, Patent WO2021233732A1-2021-11-25, 2021: Method for producing higher linear fatty acids or esters

228.	N. Sivendran, N. Pirkl, Z. Hu, A. Doppiu, L. J. Gooßen, Angew. Chem. Int. Ed., 2021, 68, 25151-25160: Halogen-bridged Methylnaphthyl Palladium Dimers as Versatile Catalyst Precursors in Coupling Reactions

227.	D. Koley, S. De, N. Sivendran, L. J. Gooßen, Chem. Eur. J., 2021, 15227-15239: Isomerization of Functionalized Olefins Using the Dinuclear Catalyst [PdI(μ-Br)(PtBu₃)]₂: A Mechanistic Study

226.	M. Dyga, C. Oppel, L. J. Gooßen, HardwareX, 2021, 10, e00211: RotoMate: An open-source, 3D printed autosampler for use with benchtop nuclear magnetic resonance spectrometers

225.	Z. Zeng, J. F. Goebel, X. Liu, L. J. Gooßen, ACS Catal., 2021, 11, 6626-6632: 2,2′-Biaryldicarboxylate Synthesis via Electrocatalytic Dehydrogenative C–H/C–H Coupling of Benzoic Acids

224.	Z. Hu, F. Belitz, G. Zhang, F. Papp, L. J. Gooßen, Org. Lett., 2021, 23, 3541-3545: Ru-Catalyzed (E)-Specific ortho-C–H Alkenylation of Arenecarboxylic Acids by Coupling with Alkenyl Bromides

223.	Z. Zeng, A. Feceu, N. Sivendran, L. J. Gooßen, Adv. Synth. Catal., 2021, 363, 2678-2722: Decarboxylation‐Initiated Intermolecular Carbon−Heteroatom Bond Formation

222.	E. Feresin, M. Kondratiuk, J. Nowack, L. J. Gooßen, Chemie in unserer Zeit, 2021, 55, 1, 28-37: Handreinigung auf molekularer Ebene – Die Rolle der Solvatation

221.	Z. Hu, X.-J. Wei, J. Handelmann, A.-K. Seitz, I. Rodstein, V. H. Gessner, L. J. Gooßen, Angew. Chem. Int. Ed., 2021, 60, 12, 6778-6783: Coupling of Reformatsky Reagents with Aryl Chlorides enabled by Ylide‐Functionalized Phosphine Ligands

220.	M. Ošeka, G. Laudadio, N. P. van Leest, M. Dyga, A. de A. Bartolomeu, L. J. Gooßen, B. de Bruin, K. T. de Oliveira, T. Noël, Chem, 2021, 7, 1, 255-266: Electrochemical Aziridination of Internal Alkenes with Primary Amines

2020

219.	M. Dyga, F. Rudolphi, L. J. Gooßen, Nachrichten aus der Chemie, 2020, 68, 27-28: Fair teilen

218.	Á. M. Martínez, D. Hayrapetyan, T. van Lingen, M. Dyga, L. J. Gooßen, Nat. Commun., 2020, 11, 4407: Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy

217.	S. De, N. Sivendran, B. Maity, N. Pirkl, D. Koley, L. J. Gooßen, ACS Catal., 2020, 10, 8, 4517-4533: Dinuclear Pd^I Catalysts in Equilibrium Isomerizations: Mechanistic Understanding, in Silico Casting, and Catalyst Development

2019

216.	X.-Q. Hu, D. Lichte, I. Rodstein, P. Weber, A.-K. Seitz, T. Scherpf, V. H. Gessner, L. J. Gooßen, Org. Lett., 2019, 21, 18, 7558–7562: Ylide-Functionalized Phosphine (YPhos)–Palladium Catalysts: Selective Monoarylation of Alkyl Ketones with Aryl Chlorides

215.	Z. Hu, X.-Q. Hu, G. Zhang, L. J. Gooßen, Org. Lett., 2019, 21, 17, 6770‑6773: Ring-Opening Ortho-C–H Allylation of Benzoic Acids with Vinylcyclopropanes: Merging Catalytic C–H and C–C Activation Concepts

214.	G. Zhang, Z. Hu, G. Bertoli, L. J. Gooßen, ACS Catal., 2019, 9, 8153-8158: Iridium-Catalyzed Synthesis of Substituted Indanones from Aromatic Carboxylates and Unsaturated Ketones

213.	P. Weber, A. Biafora, A. Doppiu, H.-J. Bongard, H. Kelm, L. J. Gooßen, Org. Process Res. Dev. 2019, 23, 1462-1470: A comparative study of dibenzylideneacetone palladium complexes in catalysis

212.	P. Weber, C. K. Rank, E. Yalcinkaya, M. Dyga, T. van Lingen, R. Schmid, F. W. Patureau, L. J. Gooßen, Adv. Synth. Catal., 2019, 361, 3925-3929: Rhodium-catalyzed ortho-Arylation of (Hetero)aromatic Acids

211.	M. S. Andrä, L. Schifferer, C. Pollok, C. Merten, L. J. Gooßen, J.-Q. Yu, Chem. Eur. J., 2019, 25, 8503-8507: Enantio‐ and Diastereoswitchable C‐H Arylation of Methylene Groups in Cycloalkanes

210.	Y. Gao, Y. Ou, L. J. Gooßen, Chem. Eur. J., 2019, 25, 8709-8712: Pd‐Catalyzed Synthesis of Vinyl Arenes from Aryl Halides and Acrylic Acid

209.	N. Pirkl, A. Del Grosso, B. Mallick, A. Doppiu, L. J. Gooßen, Chem. Commun., 2019, 55, 5275-5278: Dihalogen-bridged NHC-palladium(I) dimers: synthesis, characterisation and applications in cross-coupling reactions

208.	M. Dyga, D. Hayrapetyan, R. K. Rit, L. J. Gooßen, Adv. Synth. Catal., 2019, 361, 3548-3553: Electrochemical ipso‐Thiocyanation of Arylboron Compounds

207.	G. Zhang, Z. Hu, F. Belitz, Y. Ou, N. Pirkl, L. J. Gooßen, Angew. Chem. Int. Ed., 2019, 58, 6435-6439: Rhodium‐Catalyzed Annelation of Benzoic Acids with α,β‐Unsaturated Ketones with Cleavage of C–H, CO–OH, and C–C Bonds

206.	J. Pollini, W. M. Pankau, L. J. Gooßen, Chem. Eur. J., 2019, 25, 7416-7425: Isomerizing Olefin Metathesis

205.	M. Pichette Drapeau, J. Bahri, D. Lichte, L. J. Gooßen, Angew. Chem. Int. Ed., 2019, 58, 892-896: Decarboxylative ipso‐Amination of Activated Benzoic Acids

204.	P. Weber, T. Scherpf, I. Rodstein, D. Lichte, L. T. Scharf, L. J. Gooßen, V. H. Gessner, Angew. Chem. Int. Ed., 2019, 58, 3203-3207: A Highly Active Ylide‐Functionalized Phosphine for Palladium‐Catalyzed Aminations of Aryl Chlorides

2018

203.	J. Pollini, V. Bragoni, L. J. Gooßen, Beilstein J. Org. Chem. 2018, 14, 2737-2744: Synthesis of a tyrosinase inhibitor by consecutive ethenolysis and cross-metathesis of crude cashew nutshell liquid

202.	Y. Ou, L. J. Gooßen, Asian J. Org. Chem., 2018, 8, 650-653: Copper-Mediated Synthesis of (Diethylphosphono)difluoromethyl Thioethers from Diazonium Salts, NaSCN, and TMS-CF₂PO(OEt)₂

201.	X.-Q. Hu, Z. Hu, G. Zhang, N. Sivendran, L. J. Gooßen, Org. Lett., 2018, 20, 4337-4340: Catalytic C−N and C−H Bond Activation: ortho-Allylation of Benzoic Acids with Allyl Amines

200.	V. Bragoni, R. K. Rit, R. Kirchmann, A. S. Trita, L. J. Gooßen, Green Chem. 2018, 20, 3210-3213: Synthesis of bio-based surfactants from cashew nutshell liquid in water

199.	D. Hayrapetyan, R. K. Rit, M. Kratz, K. Tschulik, L. J. Gooßen, Chem. Eur. J., 2018, 24, 11288-11291: Electrochemical C‐H Cyanation of Electron‐Rich (Hetero)Arenes

198.	X.-Q. Hu, Z. Hu, A. S. Trita, G. Zhang, L. J. Gooßen, Chem. Sci., 2018, 9, 5289-5294: Carboxylate-directed C–H allylation with Allyl alcohols or ethers

197.	H. Li, Q. Jiang, X. Jie, Y. Shang, Y. Zhang, L. J. Gooßen, W. Su, ACS Catal., 2018, 8, 4777-4782: Rh/Cu-Catalyzed Ketone β‐Functionalization by Merging Ketone Dehydrogenation and Carboxyl-Directed C-H Alkylation

196.	G. Bertoli, B. Exner, M. V. Evers, K. Tschulik, L. J. Gooßen, J. Fluor. Chem., 2018, 210, 132-136: Metal-free trifluoromethylthiolation of arenediazonium salts with Me₄NSCF₃

195.	T. Wendling, E. Risto, T. Krause, L. J. Gooßen, Chem. Eur. J., 2018, 24, 6019-6024: Salt-Free Strategy for the Insertion of CO₂ into C-H Bonds: Catalytic Hydroxymethylation of Alkynes

194.	G. Zhang, F. Jia, L. J. Gooßen, Chem. Eur. J., 2018, 24, 4537-4541: Regioselective C–H Alkylation via Carboxylate-Directed Hydroarylation in Water

193.	S. Kovacs, B. Bayarmagnai, A. Aillerie, L. J. Gooßen, Adv. Synth. Catal., 2018, 360, 1913-1918: Practical Reagents and Methods for Nucleophilic and Electrophilic Phosphorothiolations

192.	A. S. Trita, A. Biafora, M. Pichette-Drapeau, P. Weber, L. J. Gooßen, Angew. Chem. Int. Ed., 2018, 57, 14580-14584: Regiospecific ortho-C-H Allylation of Benzoic Acids

2017

191.	L. J. Gooßen, K. F. Pfister, S. Baader, Patent WO 2017158060A1, 2017: Biofuel and method for a preparation by isomerizing metathesis

190.	K. F. Pfister, S. Baader, M. Baader, S. Berndt, L. J. Goossen, Sci. Adv., 2017, 3: Biofuel by isomerizing metathesis of rapeseed oil esters with (bio)ethylene for use in contemporary diesel engines

189.	A. Biafora, L. J. Goossen, Synlett, 2017, 28, 1885-1890: Thieme Chemistry Journals Awardees – Where Are They Now? New Reaction Mode in Carboxylate-Directed C–H Functionalizations: Carboxylates as Deciduous Directing Groups

188.	L. J. Goossen, patent DE102017214043, 2017: A process for preparing 1,4-butanediol from acethylene and carbon dioxide

187.	D. Hackenberger, P. Weber, D. C. Blakemore, L. J. Goossen, J. Org. Chem., 2017, 82, 3917-3925: Synthesis of 3-Substituted 2-Arylpyridines via Cu/Pd-Catalyzed Decarboxylative Cross-Coupling of Picolinic Acids with (Hetero)Aryl Halides

186.	A. S. Trita, L. C. Over, J. Pollini, S. Baader, S. Riegsinger, M. A. R. Meier, L. J. Goossen, Green Chem., 2017, 19, 3051-3060: Synthesis of potential bisphenol A substitutes by isomerising metathesis of renewable raw materials

185.	A. Biafora, B. A. Khan, J. Bahri, J. M. Hewer, L. J. Goossen, Org. Lett., 2017, 19, 1232–1235: Doubly Regioselective C–H Hydroarylation of Unsymmetrical Alkynes Using Carboxylates as Deciduous Directing Groups

184.	S. Kovács, B. Bayarmagnai, L. J. Goossen, Adv. Synth. Catal., 2017, 359, 250-254: Preparation of Electrophilic Trifluoromethylthio Reagents from Nucleophilic Tetramethylammonium Trifluoromethylthiolate

183.	T. Wendling, E. Risto, B. Erb, L. J. Gooßen, Green Chem., 2017, 19, 643-646: Alkoxide-Catalyzed Addition of Alkyl Carbonates across Alkynes – Stereoselective Synthesis of (E)-β-Alkoxyacrylates

182.	L. J. Goossen, M. Grünberg, patent WO 2017093427, 2017: Selective arylation method for cross-coupling of biphenyl derivatives

181.	B. Exner, B. Bayarmagnai, C. Matheis, L. J. Goossen, J. Fluor. Chem., 2017, 198, 89-93: A Synthesis of perfluoroalkyl thioethers from aromatic thiocyanates by iron-catalysed decarboxylative perfluoroalkylation

2016

180.	A. Biafora, T. Krause, D. Hackenberger, F. Belitz, L. J. Gooßen, Angew. Chem. Int. Ed., 2016, 55, 14752–14755: ortho-C–H Arylation of Benzoic Acids with Aryl Bromides and Chlorides Catalyzed by Ruthenium

179.	M. Pichette Drapeau, L. J. Gooßen, Chem. Eur. J. 2016, 22, 18654: Carboxylic Acids as Directing Groups for C−H Bond Functionalization (Minireview)

178.	J. Tang, D. Hackenberger, L. J. Gooßen, Angew. Chem. Int. Ed., 2016, 55, 11296-11299: Branched Arylalkenes from Cinnamates: Selectivity Inversion in Heck Reactions by Carboxylates as Deciduous Directing Groups

177.	C. Matheis, T. Krause, V. Bragoni, L. J. Gooßen, Chem. Eur. J., 2016, 22, 12270-12273: Trifluoromethylthiolation and Trifluoromethylselenolation of α-Diazo Esters Catalyzed by Copper

176.	C. Matheis, B. Bayarmagnai, K. Jouvin, L. J. Gooßen, Org. Chem. Front., 2016, 3, 949-952: Convenient Synthesis of Pentafluoroethyl Thioethers via Catalytic Sandmeyer Reaction with a Stable Fluoroalkylthiolation Reagent

175.	B. Erb, E. Risto, T. Wendling, L. J. Gooßen, ChemSusChem, 2016, 9, 1442-1448: Reductive Etherification of Fatty Acids or Esters with Alcohols using Molecular Hydrogen

174.	T. Krause, S. Baader, B. Erb, L. J. Gooßen, Nat. Commun., 2016, 7, 11732: Atom-economic catalytic amide synthesis from amines and carboxylic acids activated in situ with acetylenes

173.	M. F. Grünberg, F. Jia, A. Rivas-Nass, L. J. Gooßen, Adv. Synth. Catal., 2016, 358, 1589-1594: Selective Monoarylation of Primary Anilines Catalyzed by Pd(dippf) and its Application in OLED Component Synthesis

172.	L. Huang, A. Biafora, G. Zhang, V. Bragoni, L. J. Gooßen, Angew. Chem., 2016, 55, 6933-6937: Regioselective C−H Hydroarylation of Internal Alkynes with Arenecarboxylates: Carboxylates as Deciduous Directing Groups

171.	C. Matheis, V. Wagner, L. J. Gooßen, Chem. Eur. J., 2016, 22, 79-82 (hot paper): Sandmeyer-Type Trifluoromethylthiolation and Trifluoromethylselenolation of (Hetero)Aromatic Amines Catalyzed by Copper Cover Cover Profile

170.	B. Erb, M. Dierker, D. M. Ohlmann, L. J. Gooßen, Eur. J. Lipid. Sci. Tech., 2016, 118, 111-116: Selective Synthesis of Propenyl-Branched Diunsaturated Fatty Esters via Catalytic Codimerization of Ethyl Linoleate and Propylene

2015

169.	B. Exner, B. Bayarmagnai, F. Jia, L. J. Gooßen, Chem. Eur. J., 2015, 21, 17220-17223: Iron-Catalyzed Decarboxylation of Trifluoroacetate and its Application to the Synthesis of Trifluoromethyl Thioethers

168.	D. Katayev, D. Hackenberger, L. J. Gooßen, The Catalyst Review, 2015, 28, 6-11: Decarboxylative and Decarbonylative Reactions: An Industrial Perspective

167.	D. Hackenberger, B. Song, M. F. Grünberg, S. Farsadpour, F. Menges, H. Kelm, C. Groß, T. Wolff, G. Niedner-Schatteburg, W. R. Thiel, L. J. Gooßen, ChemCatChem, 2015, 7, 3579-3588: Bimetallic Cu/Pd Catalysts with Bridging Aminopyrimidinyl Phosphines for Decarboxylative Cross-Couplings at Moderate Temperatures

166.	L. Huang, D. Hackenberger, L. J. Gooßen, Angew. Chem. Int. Ed., 2015, 54, 12607-12611: Iridium-Catalyzed ortho-Arylation of Benzoic Acids with Arenediazonium Salts

165.	J. Tang, A. Biafora, L. J. Gooßen, Angew. Chem. Int. Ed., 2015, 54, 13130-13133: Catalytic Decarboxylative Cross-Coupling of Aryl Chlorides and Benzoates without Activating ortho Substituents

164.	K. Jouvin, C. Matheis, L. J. Gooßen, Chem. Eur. J., 2015, 21, 14324-14327 (hot paper): Synthesis of Aryl Tri- and Difluoromethyl Thioethers via a C-H-Thiocyanation/Fluoroalkylation Cascade

163.	M. F. Grünberg, L. J. Gooßen, WO 2015059049 A1, 2015: Monoarylation of aromatic amines

162.	C. Matheis, M. Wang, T. Krause, L. J. Gooßen, Synlett, 2015, 26, 1628-1632: Metal-Free Trifluoromethylthiolation of Alkyl Electrophiles via a Cascade of Thiocyanation and Nucleophilic Cyanide–CF3 Substitution Highlighted in Synform, 2015, 09, A122-A124

161.	D. Katayev, B. Exner, L. J. Gooßen, ChemCatChem, 2015, 7, 2028-2032: Synthesis of Biaryls by Decarboxylative Hiyama Coupling

160.	L. Huang, M. Arndt, K. Gooßen, H. Heydt, L. J. Gooßen, Chem. Rev., 2015, 115, 2596-2697: Late Transition Metal-Catalyzed Hydroamination and Hydroamidation

159.	B. Maity, L. J. Gooßen, D. Koley, Chem. Sci., 2015, 6, 2532-2552: Computational Study of the Mechanism and Selectivity of Ruthenium-Catalyzed Hydroamidations of Terminal Alkynes

158.	B. Bayarmagnai, C. Matheis, K. Jouvin, L. J. Gooßen, Angew. Chem. Int. Ed., 2015, 54, 5753-5756: Synthesis of Difluoromethyl Thioethers from Difluoromethyl Trimethylsilane and Organothiocyanates Generated in situ

2014

157.	C. Matheis, K. Jouvin, L. J. Gooßen, Org. Lett., 2014, 16, 5984-5987: Sandmeyer Difluoromethylation of (Hetero-)Arenediazonium Salts

156.	F. W. Patureau, L. J. Gooßen, Angew. Chem. Int. Ed., 2014, 53, 5738-5739: Copper-Mediated Cross-Coupling Reactions (book review)

155.	K. F. Pfister, M. F. Grünberg, L. J. Gooßen, Adv. Synth. Catal., 2014, 356, 3302-3306: Synthesis of Allylarenes via Catalytic Decarboxylation of Allyl Benzoates

154.	S. Baader, P. E. Podsiadly, D. J. Cole-Hamilton, L. J. Gooßen, Green Chem., 2014, 16, 4885-4890: Synthesis of Tsetse Fly Attractants from a Cashew Nut Shell Extract by Isomerising Metathesis

153.	G. Danoun, B. Bayarmagnai, M. F. Grünberg, C. Matheis, E. Risto, L. J. Gooßen, Synthesis, 2014, 46, 2283-2286: Sandmeyer Trifluoromethylation

152.	A. Fromm, C. van Wüllen, D. Hackenberger, L. J. Gooßen, J. Am. Chem. Soc., 2014, 136, 10007-10023: Mechanism of Cu/Pd-Catalyzed Decarboxylative Cross-Couplings: A DFT Investigation

151.	D. Katayev, K. F. Pfister, T. Wendling, L. J. Gooßen, Chem. Eur. J., 2014, 20, 9902-9905: Copper-Mediated ortho-Nitration of (Hetero)Arenecarboxylates

150.	B. Bayarmagnai, C. Matheis, E. Risto, L. J. Gooßen, Adv. Synth. Catal., 2014, 356, 2343-2348: One-Pot Sandmeyer Trifluoromethylation and Trifluoromethylthiolation

149.	J. Tang, L. J. Gooßen, Org. Lett., 2014, 16, 2664-2667: Arylalkene Synthesis via Decarboxylative Cross-Coupling of Alkenyl Halides

148.	G. Danoun, B. Bayarmagnai, M. F. Grünberg, L. J. Gooßen, Chem. Sci., 2014, 5, 1312-1316: Sandmeyer Trifluormethylthiolation of Arenediazoniumsalts with Sodium Thiocyanate and Ruppert-Prakash Reagent

147.	L. J. Gooßen, P. Mamone, G. Danoun, A. Cotte, WO 2014167017, 2014: Method for preparation of ortho-acylated (hetero)aromatic carboxylic acids

146.	L. J. Gooßen, M. Arndt, WO 2014029689, 2014: Method for producing acetylenedicarboxylic acid from acetylene and carbon dioxide

145.	L. J. Gooßen, M. Arndt, P. Mamone, M. Grünberg, US 20140187803, 2014: Method for the preparation of palladium(I) tri-tert-butylphosphine bromide dimer and process for its use in isomerization reactions

144.	L. J. Gooßen, F. Rudolphi, B. Song, A. Cotte, M. Cotta, US 20140100371, 2014: Process for preparing azomethines from alpha-oxocarboxylates, amines and aryl bromides

143.	L. J. Gooßen, T. Knauber, B. Song, A. Cotte, J. Mohr, WO 2014111493, 2014: Substituted benzimidazole phosphine compounds as ligands for palladium/copper-catalyzed decarboxylative coupling of aryl sulfonates with arenecarboxylic derivatives into biaryls

142.	L. J. Gooßen, D. Ohlmann, M. Dierker, WO 2014001101, 2014: Method for producing unsaturated compounds

2013

141.	L. J. Gooßen, D. Ohlmann, M. Dierker, US 20130340327, 2013: Process for preparing unsaturated compounds

140.	G. Danoun, P. Mamone, L. J. Gooßen, Chem. Eur. J., 2013, 19, 17287-17290: One Pot-Synthesis of 3-Alkylidenephthalides from Benzoic Acids via a Rhodium-Catalyzed ortho-C-H Acylation Process

139.	S. Bhadra, W. Dzik, L. J. Gooßen, Synthesis, 2013, 45, 2387-2390: Synthesis of Aryl Ethers from Aromatic Carboxylic Acids

138.	G. Danoun, B. Bayarmagnai, M. F. Grünberg, L. J. Gooßen, Angew. Chem. Int. Ed., 2013, 52, 7972-7975: Sandmeyer Trifluoromethylation of Arenediazonium Tetrafluoroborates

137.	S. Bhadra, C. Matheis, D. Katayev, L. J. Gooßen, Angew. Chem. Int. Ed., 2013, 52, 9279-9283: Copper-Catalyzed Dehydrogenative Coupling of Arenes and Alcohols

136.	M. F. Grünberg, L. J. Gooßen J. Organomet. Chem., 2013, 744, 140-143: Decarboxylative Allylation of Arylglyoxylic Acids with Allyl Alcohol

135.	S. Baader, D. Ohlmann, L. J. Gooßen, Chem. Eur. J., 2013, 19, 9807-9810: Isomerizing ethenolysis as an efficient strategy for styrene synthesis

134.	M. F. Grünberg, L. J. Gooßen, Chem. Eur. J., 2013, 19, 7334-7337: Synthesis of Arylacetates from Benzylic Alcohols and Oxalate Esters via Decarboxylative Coupling

133.	P. Mamone, G. Danoun, L. J. Gooßen, Angew. Chem. Int. Ed., 2013, 52, 6704-6708: Rhodium-Catalyzed ortho Acylation of Aromatic Carboxylic Acids

132.	K. S. M. Salih, P. Mamone, G. Dörr, T. O. Bauer, A. Brodyanski, C. Wagner, M. Kopnarski, R. N. Klupp Taylor, S. Demeshko, F. Mayer, V. Schünemann, S. Ernst, L. J. Gooßen, W. R. Thiel, Chem. Mater., 2013, 25, 1430-1435: Facile Synthesis of Monodisperse Maghemite and Ferrite Nanocrystals from Metal Powder and Octanoic Acid

131.	S. Bhadra, W. Dzik, L. J. Gooßen, Angew. Chem. Int. Ed., 2013, 52, 2959-2962: Synthesis of Aryl Ethers from Benzoates via Carboxylate-Directed C-H Activating Alkoxylation with Concomitant Protodecarboxylation

130.	B. Song, T. Knauber, L. J. Gooßen, Angew. Chem., 2013, 125, 3026-3030: Decarboxylierende Kreuzkupplung von Mesylaten katalysiert durch ein Kupfer/Palladium-System mit maßgeschneiderten Imidazolylphosphanliganden

129.	L. J. Gooßen, P. Mamone, Applied Homogeneous Catalysis with Organometallic Compounds: A Comprehensive Handbook, 3rd ed. (Eds.: B. Cornils, W. A. Herrmann, M. Beller), 2013: Decarbonylative and Decarboxylative Processes

128.	L. J. Gooßen, K. Gooßen, Top. Organomet. Chem.: Inventing Reactions (Ed.: L. J. Gooßen), Springer, Berlin-Heidelberg, 2013, 44, 121-141: Decarboxylative Coupling Reactions

127.	L. J. Gooßen, M. Arndt, P. Mamone, M. F. Grünberg, WO 2013000874, 2013: Method for the preparation of Palladium(I) tri-tert-butylphosphine bromide dimer and process for its use in isomerization reactions
126.	L. J. Gooßen, D. Ohlmann, M. Dierker, WO 2012055455, 2013: Forming beta-functionalized carboxylic acid esters used as substrate for isomerization reaction involves reacting in one-pot, unsaturated ester in presence of boron compound/amine and rhodium containing catalyst under oxygen-free atmosphere

125.	L. J. Gooßen, N. Rodríguez-Garrido, F. Manjolinho, P. Lange, WO 2012022801, 2013: Preparing propiolic acid or its derivative comprises reacting a terminal alkyne with carbon dioxide in the presence of a base and a copper complex having at least one ligand

2012

124.	F. Manjolinho, M. Arndt, K. Gooßen, L. J. Gooßen, ACS Catal., 2012, 2, 2014-2012: Catalytic C-H Carboxylation of Terminal Alkynes with Carbon Dioxide

123.	D. M. Ohlmann, N. Tschauder, J.-P. Stockis, K. Gooßen, M. Dierker, L. J. Gooßen, J. Am. Chem. Soc., 2012, 134, 13716-13729: Isomerizing Olefin Metathesis as a Strategy to Access Defined Distributions of Unsaturated Compounds from Fatty Acids

122.	F. Manjolinho, M. F. Grünberg, N. Rodríguez, L. J. Gooßen, Eur. J. Org. Chem., 2012, 4680-4683: Decarboxylative allylation of glyoxylic acids with diallyl carbonate

121.	P. Mamone, M. F. Grünberg, A. Fromm, B. A. Khan, L. J. Gooßen, Org. Lett., 2012, 14, 3716-3719: [Pd(μ-Br)(PtBu³)]² as a Highly Active Isomerization Catalyst: Synthesis of Enol Esters from Allylic Esters

120.	S. Bhadra, W. I. Dzik, L. J. Gooßen, J. Am. Chem. Soc., 2012, 134, 9938-9941: Decarboxylative etherification of aromatic carboxylic acids

119.	A. Cotte, M. Gotta, L. J. Gooßen, F. Rudolphi, B. Song, WO2012066134, 2012: Preparing azomethine compounds comprises reacting alpha-oxocarboxylate compounds with aryl bromide compounds and amine compounds via alpha-iminocarboxylate intermediate compounds in presence of two transition metals as catalyst

118.	W. I. Dzik, P. P. Lange, L. J. Gooßen, Chem. Sci., 2012, 3, 2671-2678: Carboxylates as Sources of Carbon Nucleophiles and Electrophiles: Comparison of Decarboxylative and Decarbonylative Pathways

117.	M. Arndt, E. Risto, T. Krause, L. J. Gooßen, ChemCatChem, 2012, 4, 484-487: Silver(I) salts in combination with DMSO: unprecedented effective catalyst systems for the carboxylation of terminal alkynes at ambient CO² pressure

116.	M. Hemgesberg, D. M. Ohlmann, Y. Schmitt, M. R. Wolfe, M. K. Müller, B. Erb, Y. Sun, L. J. Gooßen, M. Gerhards, W. R. Thiel, Eur. J. Org. Chem., 2012, 2142-2151: A Simple Access Sol-Gel Precursors Bearing Fluorescent Aromatic Core Units

115.	S. Tartaggia, O. De Lucchi, L. J. Gooßen, Eur. J. Org. Chem., 2012, 1431-1438: Practical Synthesis of Unsymmetrical Diarylacetylenes from Propiolic Acid and Two Different Aryl Bromides

114.	T. Himmler, L. J. Gooßen, F. Rudolphi, B. Song, WO 2012116942, 2012: Process for preparing aryl- and heteroarylacetic acid derivatives

113.	M. Rudzki, A. Alcalde-Aragonés, W. I. Dzik, N. Rodríguez, L. J. Gooßen, Synthesis, 2012, 44, 184-193: Selective Copper- or Silver-Catalyzed Decarboxylative Deuteration of Aromatic Carboxylic Acids

112.	B. A. Khan, A. E. Buba, L. J. Gooßen, Chem. Eur. J., 2012, 18, 1577-1581: Oxidative Trifluoromethylation of Arylboronates with Shelf-Stable Potassium (Trifluoromethyl)trimethoxyborate

111.	L. J. Gooßen, P. Mamone, C. Oppel, EP 2468708, 2012: Preparing alkyl aryl ketones comprises heating blend comprising monocarboxylic acids e.g. benzene monocarboxylic acid, iron containing catalyst and solvent e.g. sulfolane, removing water and carbon dioxide from blend, and distilling blend

110.	L. J. Gooßen, D. M. Ohlmann, M. Dierker, WO 2012143067, 2012: Process for the production of unsaturated compounds.

2011

109.	F. Rudolphi, L. J. Gooßen, J. Chem. Inf. Model., 2011, 52, 293-301: Electronic Laboratory Notebook: The Academic Point of View

108.	N. Rodríguez, F. Manjolinho, M. F. Grünberg, L. J. Gooßen, Chem. Eur. J., 2011, 17, 13688-13691: Synthesis of a,b-Unsaturated Ketones via Pd-Catalyzed Decarboxylative Allylation of a-Oxocarboxylates

107.	F. Collet, B. Song, F. Rudolphi, L. J. Gooßen, Eur. J. Org. Chem., 2011, 6486-6501: Development of Decarboxylative Coupling Processes for the Synthesis of Azomethines and Ketones

106.	W. I. Dzik, L. J. Gooßen, Angew. Chem. Int. Ed., 2011, 50, 11047-11049: Selective Crossed Tishchenko Reaction – A Waste-Free Synthesis of Benzyl Esters

105.	B. Zimmermann, W. I. Dzik, T. Himmler, L. J. Gooßen, J. Org. Chem., 2011, 76, 8107-8112: Palladium-catalyzed Cross-Coupling of Sterically Demanding Boronic Acids with a-Bromocarbonyl Compounds

104.	N. Rodríguez, L. J. Gooßen, Chem. Soc. Rev., 2011, 40, 5030-5048: Decarboxylative coupling reactions: a modern strategy for C–C-bond formation

103.	D. M. Ohlmann, L. J. Gooßen, M. Dierker, Chem. Eur. J., 2011, 17, 9508-9519: Regioselective synthesis of b-aryl- and b-amino-substituted aliphatic esters by rhodium-catalyzed tandem double-bond migration/conjugate addition

102.	B. Song, T. Himmler, L. J. Gooßen, Adv. Synth. Catal., 2011, 353, 1688-1694: Palladium/Copper-Catalyzed Di-alpha-arylation of Acetic Acid Esters

101.	M. Arndt, K. S. M. Salih, A. Fromm, L. J. Gooßen, F. Menges, G. Niedner-Schatteburg, J. Am. Chem. Soc., 2011, 133, 7428-7449: Mechanistic Investigation of the Ru-Catalyzed Hydroamidation of Terminal Alkynes

100.	B. Song, F. Rudolphi, T. Himmler, L. J. Gooßen, Adv. Synth. Catal. 2011, 353, 1565-1574: Practical Synthesis of 2-Arylacetic Acid Esters via Palladium-Catalyzed Dealkoxycarbonylative Coupling of Malonates with Aryl Halides

99.	A. E. Buba, M. Arndt, L. J. Gooßen, J. Organomet. Chem., 2011, 696, 170-178: Z-Selective Hydroamidation of Terminal Alkynes with Secondary Amides and Imides Catalyzed by a Ru/Yb-System

98.	T. Knauber, F. Arikan, G.-V. Röschenthaler, L. J. Gooßen, Chem. Eur. J., 2011, 17, 2689-2697: Copper-Catalyzed Trifluoromethylation of Aryl Iodides with Potassium (Trifluoromethyl)trimethoxyborate

97.	P. P. Lange, L. J. Gooßen, P. Podmore, T. Underwood, N. Sciammetta, Chem. Commun., 2011, 47, 3628-3630: Decarboxylative biaryl synthesis in a continuous flow reactor

96.	L. J. Gooßen, F. Rudolphi, Chemie in unserer Zeit., 2011, 45, 56-57: Open Source Program: An Electronic Labjournal

95.	F. Rudolphi, B. Song, L. J. Gooßen, Adv. Synth. Catal., 2011, 353, 337-342: Synthesis of Azomethines from a-Oxocarboxylates, Amines and Aryl Bromides via One-Pot Three-Component Decarboxylative Coupling

94.	L. J. Gooßen, T. Knauber, EP 2366680, 2011: Process for the synthesis of 4-haloalkyl-biphenyl-2-carboxylic acids

93.	T. Himmler, L. J. Gooßen, B. Zimmermann, WO 2011089072, 2011: Process for the preparation of aryl- and heteroarylacetic acid derivatives

92.	L. J. Gooßen, P. Mamone, C. Oppel, Adv. Synth. Catal., 2011, 353, 57-63: Catalytic Decarboxylative Cross-Ketonisation of Aryl- and Alkylcarboxylic Acids using Magnetite Nanoparticles

2010

91.	F. Rudolphi, L. J. Gooßen, Nachr. Chem., 2010, 5, 548-550: Ein elektronisches Laborjournal als Open-Source-Software

90.	F. Rudolphi, L. J. Gooßen, M. Stesycki, Chemie Report, 2010, 5, 16-17: Leistungsstark und durchdacht - Fonds-Stipendiat entwickelt elektronisches Laborjournal

89.	L. J. Gooßen, B. A. Khan, T. Fett, M. Treu, Adv. Synth. Catal., 2010, 352, 2166-2170: Low-pressure Hydrogenation of Arenecarboxylic Acids to Aryl Aldehydes

88.	L. J. Gooßen, F. Collet, K. Gooßen, Isr. J. Chem., 2010, 50, 617-629: Decarboxylative Coupling Reactions

87.	L. J. Gooßen, N. Rodríguez, K. Gooßen, McGraw-Hill Yearbook of Science and Technology, 2010: Decarboxylative Couplings

86.	L. J. Gooßen, N. Rodríguez, F. Manjolinho, P. P. Lange, Adv. Synth. Catal., 2010, 352, 2913-2917: Synthesis of Propiolic Acids via Cu-catalyzed Insertion of Carbon Dioxide into the C–H bond of Terminal Alkynes

85.	L. J. Gooßen, M. Blanchot, M. Arndt, K. S. M. Salih, Synlett, 2010, 1685-1687: Synthesis of Botryllamides and Lansiumamides via Ru-Catalyzed Hydroamidation of Alkynes

84.	L. J. Gooßen, B. Zimmermann, T. Knauber, Beilstein J. Org. Chem., 2010, 6, No. 43.: Pd-catalyzed decarboxylative Heck vinylation of 2-nitrobenzoates in the presence of CuF²

83.	L. J. Gooßen, N. Rodríguez, C. Linder, P. P. Lange, A. Fromm, ChemCatChem, 2010, 2, 430-442: Comparative Study of Copper- and Silver-Catalyzed Protodecarboxylations of Carboxylic Acids

82.	L. J. Gooßen, P. P. Lange, N. Rodríguez, C. Linder, Chem. Eur. J., 2010, 16, 3906-3909: Low-Temperature Ag/Pd-Catalyzed Decarboxylative Cross-Coupling of Aryl Triflates with Aromatic Carboxylate Salts

81.	L. J. Gooßen, D. M. Ohlmann, M. Dierker, Green Chem., 2010, 12, 197-200: Silver Triflate-Catalysed Synthesis of γ-Lactones from Fatty Acids (Cover)

80.	L. J. Gooßen, N. Rodríguez, P. P. Lange, C. Linder, Angew. Chem. Int. Ed., 2010, 49, 1111-1114: Decarboxylative Cross-Coupling of Aryl Tosylates with Aromatic Carboxylate Salts

79.	L. J. Gooßen, D. M. Ohlmann, M. Dierker, T. Löhl, EP 10/2241562, 2010: Process for the production of lactones

2009

78.	L. J. Gooßen, N. Rodríguez, K. Gooßen, Angew. Chem. Int. Ed., 2009, 48, 9592-9594: Stereoselective Synthesis of α-Chlorovinyl Ketones or Arenes by Catalytic Additions of Acid Chlorides to Alkynes Angew. Chem. Int. Ed. 2009, 48, 9592-9594: Stereoselective Synthesis of α-Chlorovinyl Ketones or Arenes by Catalytic Additions of Acid Chlorides to Alkynes.

77.	L. J. Gooßen, C. Linder, N. Rodríguez, P. P. Lange, A. Fromm, Chem. Commun., 2009, 7173-7175: Silver-catalysed protodecarboxylation of carboxylic acids

76.	L. J. Gooßen, M. Blanchot, K. S. M. Salih, K. Gooßen, Synthesis, 2009, 13, 2283-2288: Ruthenium-Catalyzed Addition of Primary Amides to Alkynes: A Stereoselective Synthesis of Secondary Enamides Synfacts 2009, 1, 85.

75.	L. J. Gooßen, C. Linder, N. Rodríguez, P. P. Lange, Chem. Eur. J., 2009, 15, 9336-9349 (Frontispiece): Biaryl and Aryl Ketone Synthesis via Pd-Catalyzed Decarboxylative Coupling of Carboxylate Salts with Aryl Triflates

74.	L. J. Gooßen, K. Gooßen, C. Stanciu, Angew. Chem. Int. Ed., 2009, 48, 3569-3571: Aryl-C–O-activation of Aryl Carboxylates in Nickel-Catalyzed Biaryl Syntheses

73.	L. J. Gooßen, B. Zimmermann, C. Linder, N. Rodríguez, P. P. Lange, J. Hartung, Adv. Synth. Catal., 2009, 351, 2667-2674: Synthesis of Biaryls and Aryl Ketones via Microwave-Assisted Decarboxylative Cross-Couplings

72.	L. J. Gooßen, F. Manjolinho, B. A. Khan, N. Rodríguez, J. Org. Chem., 2009, 74, 2620-2623: Microwave assisted Cu-catalyzed protodecarboxylation of aromatic carboxylic acids

71.	L. J. Gooßen, D. M. Ohlmann, P. P. Lange, Synthesis, 2009, 160-164: The Thermal Amidation of Carboxylic Acids Revisited

70.	A. Cotté, M. Gotta, L. J. Gooßen, F. Rudolphi, C. Oppel, N. Rodríguez, EP 09/2096101, 2009: Method for producing ketones from alpha-oxocarboxylates and aryl bromides

2008

69.	L. J. Gooßen, M. Arndt, M. Blanchot, F. Rudolphi, F. Menges, G. Niedner-Schatteburg, Adv. Synth. Catal., 2008, 350, 2701-2707: A practical and effective RuCl³-based protocol for the regio- and stereoselective catalytic hydroamidation of terminal alkynes

68.	L. J. Gooßen, T. Knauber, J. Org. Chem., 2008, 73, 8631-8634: Concise Synthesis of Telmisartan via Decarboxylative Cross-Coupling

67.	L. J. Gooßen, N. Rodriguez, C. Linder, J. Am. Chem. Soc., 2008, 130, 15248-15249: Decarboxylative Biaryl Synthesis from Aromatic Carboxylates and Aryl Triflates

66.	L. J. Gooßen, M. Blanchot, K. S. M. Salih, R. Karch, A. Rivas-Nass, Org. Lett., 2008, 10, 4497-4499: Ruthenium-Catalyzed Stereoselective anti-Markovnikov-Addition of Thioamides to Alkynes

65.	L. J. Gooßen, K. S. M. Salih, M. Blanchot, Angew. Chem. Int. Ed., 2008, 47, 8492-8495: Synthesis of Secondary Enamides via Ru-Catalyzed Selective Addition of Amides to Terminal Alkynes

64.	L. J. Gooßen, B. Zimmermann, T. Knauber, Angew. Chem. Int. Ed., 2008, 47, 7103-7106: Pd/Cu-catalyzed decarboxylative cross-coupling of aryl chlorides and potassium carboxylates

63.	L. J. Gooßen, N. Rodríguez, C. Linder, B. Zimmermann, T. Knauber, Org. Synth., 2008, 85, 196-204: Synthesis of 2-Substituted Biaryls via Cu/Pd-Catalyzed Decarboxylative Cross-Coupling of 2-Substituted Potassium Benzoates

62.	L. J. Gooßen, K. Gooßen, N. Rodríguez, M. Blanchot, C. Linder, B. Zimmermann, Pure Appl. Chem., 2008, 80, 1725-1731: New Catalytic Transformations of Carboxylic Acids

61.	L. J. Gooßen, K. Gooßen, Aktuelle Wochenschau der GDCh, 2008, 18: Dream Reactions – Nachhaltigkeit durch atomökonomische Synthesen
60.	L. J. Gooßen, N. Rodríguez, K. Gooßen, Angew. Chem. Int. Ed., 2008, 47, 3100 – 3120: Carboxylic acids as substrates in homogeneous catalysis

59.	L. J. Gooßen, F. Rudolphi, C. Oppel, N. Rodríguez, Angew. Chem. Int. Ed., 2008, 47, 3043–3045: Synthesis of Ketones from a-Oxocarboxylates and Aryl Bromides by Cu/Pd-Catalyzed Decarboxylative Cross-Coupling

58.	A. Cotté, N. Mueller, L. Rodefeld, L. J. Gooßen, C. Linder, WO 08/122555, 2008: 2-Nitro-5-fluor-3’,4’-dichlorbiphenyl sowie ein Verfahren zu dessen Herstellung

2007

57.	L. J. Gooßen, N. Rodríguez, Angew. Chem. Int. Ed., 2007, 46, 7544-7546: Heterodimerization of Olefins: A Highly Promising Strategy for the Selective Synthesis of Functionalized Alkenes

56.	L. J. Gooßen, B. Melzer, J. Org. Chem., 2007, 72, 7473-7476: Synthesis of Valsartan via Decarboxylative Biaryl Coupling

55.	L. J. Gooßen, W. R. Thiel, N. Rodríguez, C. Linder, B. Melzer, Adv. Synth. Catal., 2007, 349, 2241-2246: Cu-catalyzed protodecarboxylation of aromatic carboxylic acids.

54.	L. Gooßen, Angew. Chem. Int. Ed., 2007, 46, 3791-3792: Metal-Catalysis in Industrial Organic Processes. Edited by Gian Paolo Chiusoli and Peter M. Maitlis (book review)

53.	L. J. Gooßen, N. Rodríguez, B. Melzer, C. Linder, G. Deng, L. M. Levy, J. Am. Chem. Soc., 2007, 129, 4824-4833: Biaryl Synthesis via Pd-Catalyzed Decarboxylative Coupling of Aromatic Carboxylates with Aryl Halides

2006 and earlier

52.	L. J. Gooßen, M. Blanchot, C. Brinkmann, K. Gooßen, R. Karch, A. Rivas‑Nass, J. Org. Chem., 2006, 71, 9506-9509: Ru-Catalyzed Stereoselective Addition of Imides to Alkynes

51.	L. J. Gooßen, C. Linder, Synlett, 2006, 3489-3491: Catalytic reductive etherification of ketones with alcohols at ambient hydrogen pressure: A practical, waste-minimized synthesis of dialkyl ethers

50.	L. J. Gooßen, G. Deng, L. M. Levy, Science, 2006, 313, 662-664: Synthesis of Biaryls via Catalytic Decarboxylative Coupling

49.	L. J. Gooßen, Koley, H. Hermann, W. Thiel, Organometallics, 2006, 25, 54-67: Palladium Monophosphine Intermediates in Catalytic Cross-Coupling Reactions: A DFT Study

48.	L. J. Gooßen, K. Baumann, The Heck Reaction in: Handbook of C-H Transformations: Applications in Organic Synthesis (G. Dyker, Ed.), Wiley-VCH, Weinheim, 2005

47.	L. J. Gooßen, G. Deng, WO 06/136135, 2006: Verfahren zur decarboxylierenden C-C Verknüpfung von Carbonsäuren mit Kohlenstoffelektrophilen

46.	L. J. Gooßen, D. Koley, H. Hermann, W. Thiel, J. Am. Chem. Soc., 2005, 127, 11102-11114: The Palladium-Catalyzed Cross-Coupling Reaction of Carboxylic Anhydrides with Arylboronic Acids: A DFT Study

45.	L. J. Gooßen, D. Koley, H. Hermann, W. Thiel, Organometallics, 2005, 24, 2398-2410: Mechanistic Pathways for Oxidative Addition of Aryl Halides to Palladium(0) Complexes: A DFT Study

44.	L. J. Gooßen, J. E. Rauhaus, G. Deng, Angew. Chem., 2005, 117, 4110-4113: Ru-catalyzed anti-Markovnikov addition of amides to alkynes: A regio- and stereoselective synthesis of enamides

43.	L. J. Gooßen, M. K. Dezfuli, Synlett, 2005, 445-448: Practical Protocol for the Palladium-Catalyzed Synthesis of Arylphosphonates from Bromoarenes and Diethyl Phosphite

42.	L. J. Gooßen, J. Paetzold, O. Briel, A. Rivas-Nass, Synlett, 2005, 275-278: Buchwald-Hartwig Aminations of Aryl Chlorides: A Practical Protocol Based on Commercially Available Pd(0)-NHC Catalysts

41.	L. J. Gooßen, J. E. Rauhaus, WO 06/056166, 2006, 21, 17220-17223: Verfahren zur Addition von Amiden, Harnstoffen, Lactamen und Carbamaten an Alkine

40.	L. J. Gooßen, J. Paetzold, Adv. Synth. Catal., 2004, 346, 1665-1668: New Synthesis of Biaryls via Rh-catalyzed Decarbonylative Suzuki-Coupling of Carboxylic Anhydrides with Arylboroxines

39.	L. J. Gooßen, Appl. Organomet. Chem., 2004, 18, 602-604: A Simple and Practical Protocol for the Pd-Catalyzed Cross-Coupling of Boronic Acids with Methyl Iodide

38.	L. J. Gooßen, D. Koley, H. Hermann, W. Thiel, Chem. Commun., 2004, 2141-2143: The Mechanism of the Oxidative Addition of Aryl Halides to Pd-Catalysts: A DFT Investigation

37.	L. J. Gooßen, N. Rodriguez, Chem. Commun., 2004, 724-725: A Mild and Efficient Protocol for the Conversion of Carboxylic Acids to Olefins by a Catalytic Decarbonylative Elimination Reaction

36.	L. J. Gooßen, A. Döhring, Synlett, 2004, 263-266: A Convenient Protocol for the Esterification of Carboxylic Acids with Alcohols in the Presence of Di-t-butyl Dicarbonate

35.	L. J. Gooßen, J. Paetzold, Angew. Chem. Int. Ed., 2004, 43, 1095-1098: Decarbonylative Heck Olefination of Enol Esters: Salt-Free and Environmentally Friendly Access to Vinyl Arenes

34.	M. T. Reetz, L. J. Gooßen, A. Meiswinkel, J. Paetzold, J. Feldthusen Jensen, Org. Lett., 2003, 5, 3099-3101: Enantioselective Rh-Catalyzed Hydrogenation of Vinyl Carboxylates using Monodentate Phosphite Ligands

33.	L. J. Gooßen, A. Döhring, Adv. Synth. Catal., 2003, 345, 943-947: Lewis Acids as Highly Efficient Catalysts for the Decarboxylative Esterification of Carboxylic Acids with Dialkyl Dicarbonates

32.	L. J. Gooßen, J. Paetzold, D. Koley, Chem. Commun., 2003, 706-707: Regiocontrolled Ru-catalyzed Addition of Carboxylic Acids to Alkynes: Practical Protocols for the Synthesis of Vinyl Esters

31.	L. J. Gooßen, Angew. Chem., 2002, 114, 3929-3932: Asymmetrische Hydrovinylierung: neue perspektiven durch modulare Ligandensysteme (Highlight) Angew. Chem. Int. Ed., 2002, 41, 3775-3778: Asymmetric Hydrovinylation: New Perspectives through Use of Modular Ligand Systems

30.	L. J. Gooßen, Angew. Chem. Int. Ed., 2002, 41, 2845-2846: Cross-Coupling Reactions - A Practical Guide (book review)

29.	L. J. Gooßen, J. Paetzold, L. Winkel, Synlett, 2002, 1721-1723: Pd-Catalyzed Decarbonylative Heck Olefination of Aromatic Carboxylic Acids activated in situ with Di-tert-butyl Dicarbonate

28.	L. J. Gooßen, L. Winkel, A. Döhring, K. Ghosh, J. Paetzold, Synlett, 2002, 1237-1240: Pd-Catalyzed Synthesis of Functionalized Arylketones from Boronic Acids and Carboxylic Acids Activated in situ with Dimethyl Dicarbonate

27.	L. J. Gooßen, K. Ghosh, Eur. J. Org. Chem., 2002, 19, 3254-3256: Palladium-Catalyzed Synthesis of Arylketones from Boronic Acids and Carboxylic Acids Activated in situ by Pivalic Acid Anhydride

26.	L. J. Gooßen, K. Ghosh, Chem. Commun., 2002, 836-837: New Pd-Catalyzed Selective Reduction of Carboxylic Acids to Aldehydes

25.	L. J. Gooßen, J. Paetzold, WO 03/043958, 2003: Verfahren zur Herstellung von Vinylarenen und 1,3-Dienen aus Aryl- bzw. Vinylcarbonsäurederivaten

24.	L. J. Gooßen, J. Paetzold, Angew. Chem. Int. Ed., 2002, 41, 1237-1241: Pd‑Catalyzed Decarbonylative Olefination of Aryl Esters: Towards a Waste-Free Heck Reaction

23.	L. J. Gooßen, K. Baumann, Chemie in unserer Zeit, 2001, 35, 402-403: Asymmetrische Katalyse

22.	L. J. Gooßen, K. Ghosh, Chem. Commun. 2001, 20, 2084-2085: A New Practical Ketone Synthesis Directly from Carboxylic Acids: First Application of Coupling Reagents in Palladium Catalysis

21.	L. J. Gooßen, K. Ghosh (Studiengesellschaft Kohle m.b.H.), WO 02/092547, 2002: Verfahren zur Herstellung von Ketonen aus Carbonsäureanhydriden

20.	L. J. Gooßen, Angew. Chem. Int. Ed., 2001, 40, 3458-3460: Palladium-Catalyzed Synthesis of Aryl Ketones from Boronic Acids and Carboxylic Acids or Anhydrides

19.	L. J. Gooßen (Studiengesellschaft Kohle m.b.H.), WO 02/072524, 2002: Verfahren zur Herstellung von Vinyl-, Aryl- und Heteroarylessigsäuren und ihrer Derivate

18.	L. J. Gooßen, Chem. Commun., 2001, 7, 669-670: Palladium-Catalyzed Synthesis of Arylacetic Acid Derivatives from Boronic Acids

17.	L. J. Gooßen, A. S. Ferwanah, Synlett, 2000, 2000, 1801-1803: A Mild and Efficient Protocol for the Catalytic Silylation of Aryl Bromides

16.	L. J. Gooßen, C. Heinemann, M. Jautelat, H. Greiving (Bayer AG), DE 10061202, 2002: Epoxidation and Hydrogenation Procedure for the Production of 1,6-Hexanediol from 1,5-Hexadiene

15.	C. Heinemann, M. Jautelat, O. Kuhn, L. J. Gooßen, D. Ganzer (Bayer AG), DE 10064751, 2002: Verfahren zur Herstellung von Alk-3-en-1-olen

14.	L. J. Gooßen, M. Jautelat, C. Heinemann, H. Greiving, K. Urtel, O. Kuhn (Bayer AG), patent WO 02/051780, 2002: Verfahren zur Herstellung von 1,6-Hexandiolen

13.	L. J. Gooßen, M. Hendrix (Bayer AG), EP 1157995, 2001: Preparation of Immobilized Palladium Complexes as Catalysts

12.	L. J. Gooßen, H. Liu, K. R. Dress, K. B. Sharpless, Angew. Chem. Int. Ed., 1999, 38, 1080-1083: Catalytic Asymmetric Aminohydroxylation with Amino-Substituted Heterocycles as Nitrogen Sources

11.	L. J. Gooßen, H. Liu, K. R. Dress, K. B. Sharpless, WO 00/10977, 2000: Catalytic Aminohydroxylation Using Amino-Substituted Heterocycles

10.	K. R. Dress, L. J. Gooßen, H. Liu, D. Jerina, K. B. Sharpless, Tetrahedron Lett., 1998, 39, 7669-7672: Catalytic Aminohydroxylation with Adenine-Derivatives as Nitrogen Sources

9.	L. J. Gooßen, Funktionalisierte Imidazolin-2-yliden-Metallkomplexe in der Katalyse, Hieronymus Verlag, München 1997, ISBN: 3-928286-88-9

8.	W. A. Herrmann, L. J. Gooßen, M. Spiegler, Organometallics, 1998, 17, 2162-2168: Chiral Imidazoline-2-ylidene-Oxazoline Metal Complexes

7.	W. A. Herrmann, L. J. Gooßen, M. Spiegler, J. Organomet. Chem., 1997, 547, 357-366: Functionalized Imidazoline-2-ylidene Complexes of Rhodium and Palladium

6.	W. A. Herrmann, L. J. Gooßen, G. R. J. Artus, C. Köcher, Organometallics, 1997, 16, 2472-2477: Transition-Metal-Complexes of Chiral Imidazoline-2-ylidene Ligands

5.	W. A. Herrmann, L. J. Gooßen, C. Köcher, G. R. J. Artus, Angew. Chem. Int. Ed., 1996, 35, 2805-2807: Chiral Heterocylic Carbenes in Asymmetric Homogeneous Catalysis

4.	W. A. Herrmann, C. Köcher, L. J. Gooßen, G. R. J. Artus, WO 97/34875, 1997: Verfahren zur Herstellung heterocyclischer Carbene

3.	W. A. Herrmann, C. Köcher, L. J. Gooßen, G. R. J. Artus, Chem. Eur. J., 1996, 2, 1627-1636: A High-Yielding Synthesis of Novel Functionalized N-Heterocyclic Carbenes in Liquid Ammonia

2.	M. D. Curtis, S. Druker, L. J. Gooßen, J. Kampf, Organometallics, 1997, 16, 231-235: Structures of Anionic Mo/Co/S Cluster Salts.

1.	J. Ashe III, L. J. Gooßen, J. Kampf, H. Konishi, Angew. Chem. Int. Ed., 1992, 31, 1642-1643: The First Stibepine: Synthesis and Structure of Sb-Chlorobenzo[d]stibepine

Organic Chemistry - Prof. Gooßen

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