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Gertrud Auer - Publications

Affiliations: 
2002-2006 Albert-Ludwigs-Universität Freiburg, Freiburg im Breisgau, Baden-Württemberg, Germany 
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13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2008 Rendler S, Plefka O, Karatas B, Auer G, Fröhlich R, Mück-Lichtenfeld C, Grimme S, Oestreich M. Stereoselective alcohol silylation by dehydrogenative Si-O coupling: scope, limitations, and mechanism of the cu-h-catalyzed non-enzymatic kinetic resolution with silicon-stereogenic silanes. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 11512-28. PMID 19021177 DOI: 10.1002/Chem.200801377  0.651
2006 Walter C, Auer G, Oestreich M. Rhodium-catalyzed enantioselective conjugate silyl transfer: 1,4-addition of silyl boronic esters to cyclic enones and lactones. Angewandte Chemie (International Ed. in English). 45: 5675-7. PMID 16858702 DOI: 10.1002/Anie.200601747  0.629
2006 Auer G, Oestreich M. Silylzincation of carbon-carbon multiple bonds revisited. Chemical Communications (Cambridge, England). 311-3. PMID 16391744 DOI: 10.1039/B513528A  0.47
2006 Oestreich M, Walter C, Auer G. Rh-Catalyzed Enantioselective 1,4-Addition of Silyl Boronic Esters Synfacts. 2006: 1142-1142. DOI: 10.1055/S-2006-949435  0.635
2006 Auer G, Weiner B, Oestreich M. Copper-free and copper-promoted conjugate addition reactions of bis(triorganosilyl) zincs and tris(triorganosilyl) zincates Synthesis. 2113-2116. DOI: 10.1055/S-2006-942405  0.482
2006 Walter C, Auer G, Oestreich M. Rhodiumkatalysierter enantioselektiver konjugierter Silyltransfer: 1,4-Addition von Silylboronsäureestern an cyclische Enone und Lactone Angewandte Chemie. 118: 5803-5805. DOI: 10.1002/Ange.200601747  0.65
2006 Rendler S, Auer G, Keller M, Oestreich M. Preparation of a privileged silicon-stereogenic silane: Classical versus kinetic resolution Advanced Synthesis and Catalysis. 348: 1171-1182. DOI: 10.1002/Adsc.200606071  0.736
2005 Rendler S, Auer G, Oestreich M. Kinetic resolution of chiral secondary alcohols by dehydrogenative coupling with recyclable silicon-stereogenic silanes. Angewandte Chemie (International Ed. in English). 44: 7620-4. PMID 16252303 DOI: 10.1002/Anie.200502631  0.723
2005 Rendler S, Auer G, Oestreich M. Kinetische Racematspaltung von chiralen sekundären Alkoholen durch dehydrierende Kupplung mit zurückgewinnbaren, siliciumstereogenen Silanen Angewandte Chemie. 117: 7793-7797. DOI: 10.1002/Ange.200502631  0.658
2005 Oestreich M, Auer G. Practical synthesis of allylic silanes from allylic esters and carbamates by stereoselective copper-catalyzed allylic substitution reactions Advanced Synthesis and Catalysis. 347: 637-640. DOI: 10.1002/Adsc.200404381  0.555
2004 Oestreich M, Auer G, Keller M. On the mechanism of the reductive metallation of asymmetrically substituted silyl chlorides European Journal of Organic Chemistry. 184-195. DOI: 10.1002/Ejoc.200400622  0.51
2004 Oestereich M, Schmid UK, Auer G, Keller M. A Convergent Method for the Synthesis of Highly Enantiomerically Enriched Cyclic Silanes with Silicon-Centered Chirality Cheminform. 35. DOI: 10.1002/chin.200411258  0.34
2003 Oestreich M, Schmid UK, Auer G, Keller M. A Convergent Method for the Synthesis of Highly Enantiomerically Enriched Cyclic Silanes with Silicon-Centered Chirality Synthesis. 2003: 2725-2739. DOI: 10.1055/S-2003-42477  0.586
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