Publikationen von L. J. Goossen

Goossen, L. J.; Koley, D.; Hermann, H. L.; Thiel, W. Palladium monophosphine intermediates in catalytic cross-coupling reactions: A DFT study. Organometallics 2006, 25, 54–67.

Goossen, L. J.; Dezfuli, M. K. Practical protocol for the palladium-catalyzed synthesis of arylphosphonates from bromoarenes and diethyl phosphite. Synlett 2005, Nr. 3, 445–448.

Goossen, L. J.; Koley, D.; Hermann, H. L.; Thiel, W. Mechanistic pathways for oxidative addition of aryl halides to palladium(0) complexes: A DFT study. Organometallics 2005, 24, 2398–2410.

Goossen, L. J.; Koley, D.; Hermann, H. L.; Thiel, W. The palladium-catalyzed cross-coupling reaction of carboxylic anhydrides with arylboronic acids: A DFT study. Journal of the American Chemical Society 2005, 127, 11102–11114.

Goossen, L. J.; Paetzold, J.; Briel, O.; Rivas-Nass, A.; Karch, R.; Kayser, B. Buchwald-Hartwig aminations of aryl chlorides: A practical protocol based on commercially available Pd(0)-NHC catalysts. Synlett 2005, Nr. 2, 275–278.

Goossen, L. J.; Rauhaus, J. E.; Deng, E. Ru-catalyzed anti-Markovnikov addition of amides to alkynes: a regio- and stereoselective synthesis of enamides. Angewandte Chemie 2005, 117, 4110–4113.

Goossen, L. J.; Rauhaus, J. E.; Deng, G. J. Ru-catalyzed anti-Markovnikov addition of amides to alkynes: A regio- and stereoselective synthesis of enamides. Angewandte Chemie-International Edition 2005, 44, 4042–4045.

Gooßen, L. J. A simple and practical protocol for the palladium-catalyzed cross-coupling of boronic acids with methyl iodide. Applied Organometallic Chemistry 2004, 18, 602–604.

Gooßen, L. J.; Döhring, A. A convenient protocol for the esterification of carboxylic acids with alcohols in the presence of di-t-butyl dicarbonate. Synlett 2004, Nr. 2, 263–266.

Gooßen, L. J.; Koley, D.; Hermann, H.; Thiel, W. The mechanism of the oxidative addition of aryl halides to Pd-catalysts: a DFT investigation. Chemical Communications (Cambridge, U. K.) 2004, Nr. 19, 2141–2143.

Gooßen, L. J.; Paetzold, J. Decarbonylative heck olefination of enol esters: Salt-free and environmentally friendly access to vinyl arenes. Angewandte Chemie-International Edition 2004, 43, 1095–1098.

Gooßen, L. J.; Paetzold, J. New synthesis of biaryls via Rh-catalyzed decarbonylative Suzuki-coupling of carboxylic anhydrides with arylboroxines. Advanced Synthesis & Catalysis 2004, 346, 1665–1668.

Gooßen, L. J.; Paetzold, J. Decarbonylierende Heck-Olefinierung von Enolestern: ein salzfreier und umweltfreundlicher Zugang zu Vinylarenen. Angewandte Chemie 2004, 116, 1115–1118.

Gooßen, L. J.; Rodriguez, N. A mild and efficient protocol for the conversion of carboxylic acids to olefins by a catalytic decarbonylative elimination reaction. Chemical Communications (Cambridge, U. K.) 2004, Nr. 6, 724–725.

Reetz, M. T.; Gooßen, L. J.; Meiswinkel, A.; Paetzold, J.; Feldthusen Jensen, J. Enantioselective Rh-catalyzed hydrogenation of vinyl carboxylates with monodentate phosphite ligands. Organic Letters 2003, 5, 3099–3101.

Gooßen, L. J.; Döhring, A. Lewis acids as highly efficient catalysts for the decarboxylative esterification of carboxylic acids with dialkyl dicarbonates. Advanced Synthesis & Catalysis 2003, 345, 943–947.

Gooßen, L. J.; Paetzold, J.; Koley, D. Regiocontrolled Ru-catalyzed addition of carboxylic acids to alkynes: practical protocols for the synthesis of vinyl esters. Chemical Communications (Cambridge, U. K.) 2003, Nr. 6, 706–707.

Gooßen, L. J.; Ghosh, K. Palladium-catalyzed synthesis of aryl ketones from boronic acids and carboxylic acids activated in situ by pivalic anhydride. European Journal of Organic Chemistry 2002, Nr. 19, 3254–3267.

Gooßen, L. J.; Paetzold, J.; Winkel, L. Pd-catalyzed decarbonylative Heck olefination of aromatic carboxylic acids activated in situ with di-tert-butyl dicarbonate. Synlett 2002, Nr. 10, 1721–1723.

Gooßen, L. J.; Winkel, L.; Döhring, A.; Ghosh, K.; Paetzold, J. Pd-catalyzed synthesis of functionalized arylketones from boronic acids and carboxylic acids activated in situ with dimethyl dicarbonate. Synlett 2002, Nr. 8, 1237–1240.