139139-89-2Relevant articles and documents
Enantioselective chlorinative aldol reaction of α-substituted acroleins catalyzed by chiral phosphine oxides
Kotani, Shunsuke,Hanamure, Takuya,Nozaki, Hirono,Sugiura, Masaharu,Nakajima, Makoto
supporting information, p. 282 - 287 (2017/02/18)
The enantioselective chlorinative aldol reaction of α-substituted acroleins with aldehydes catalyzed by chiral phosphine oxides is described. A hypervalent silicon complex-derived chloride adds to the α-substituted acroleins to form the corresponding sily
Process for producing optically active carboxylic acid
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, (2008/06/13)
A process for the production of an optically active carboxylic acid (I), which comprises subjecting an olefinic carboxylic acid (II) to asymmetric hydrogenation using a complex as a catalyst consisting of an optically active phosphine (III) and a ruthenium compound. Complex of STR1 with a ruthenium compound STR2 According to the process of the present invention, optically active carboxylic acids can be produced with high yield.
2,2'-bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl and transition metal complex containing the same as ligand
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, (2008/06/13)
2,2'-Bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl represented by formula (I). STR1 is disclosed. A transition metal complex containing the same, a process for producing 2,2'-Bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl, and a process for producing 2,2'-bis(diphenylphosphinyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl are also disclosed.