Ruthenium-Catalyzed Regio- and Stereoselective Addition of Carboxylic Acids to Aryl and Trifluoromethyl Group Substituted Unsymmetrical Internal Alkynes
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Kawatsura, Motoi
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Tottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, JapanTottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, Japan
Kawatsura, Motoi
[1
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Namioka, Junya
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Tottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, JapanTottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, Japan
Namioka, Junya
[1
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Kajita, Koji
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Tottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, JapanTottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, Japan
Kajita, Koji
[1
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Yamamoto, Mitsuaki
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Tottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, JapanTottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, Japan
Yamamoto, Mitsuaki
[1
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Tsuji, Hiroaki
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Tottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, JapanTottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, Japan
Tsuji, Hiroaki
[1
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Itoh, Toshiyuki
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Tottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, JapanTottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, Japan
Itoh, Toshiyuki
[1
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[1] Tottori Univ, Grad Sch Engn, Dept Chem & Biotechnol, Tottori 6808552, Japan
The regio- and stereoselective addition of carboxylic acids to aryl and trifluoromethyl group substituted unsymmetrical Internal alkynes has been accomplished: the Ru-3(CO)(12)/3PPh(3) catalyst system has effectively catalyzed the reaction to afford the trifluoromethyl group substituted (E)-enol esters with high regio- and stereoselectivities.
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Univ Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, FranceUniv Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, France
Rivera-Hernandez, Alejandro
Fallon, Brendan J.
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Univ Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, FranceUniv Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, France
Fallon, Brendan J.
Ventre, Sandrine
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Univ Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, FranceUniv Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, France
Ventre, Sandrine
Simon, Cedric
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Univ Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, FranceUniv Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, France
Simon, Cedric
Tremblay, Marie-Helene
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Univ Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, FranceUniv Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, France
Tremblay, Marie-Helene
Gontard, Geoffrey
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Univ Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, FranceUniv Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, France
Gontard, Geoffrey
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Derat, Etienne
Amatore, Muriel
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Univ Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, FranceUniv Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, France
Amatore, Muriel
Aubert, Corinne
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Univ Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, FranceUniv Paris 06, Inst Parisien Chim Mol, UMR CNRS 8232, Case 229,4 Pl Jussieu, F-75252 Paris 05, France