Conformationally Flexible Biphenyl‐phosphane Ligands for Ru‐Catalyzed Enantioselective Hydrogenation
摘要:
Stereomutation of a BIPHEP/RuCl 2 /diamine complex (shown schematically) is possible because of the conformational flexibilty of BIPHEP ligands. The result is an asymmetric activation in the Ru-catalyzed hydrogenation of carbonyl compounds to optically active alcohols. Whereas a racemic BINAP/RuCl 2 complex with a chiral diamine activator gives a 1:1 mixture of two diastereomers, unequal amounts of the diastereomers can be produced from a BIPHEP/RuCl 2 complex and a chiral diamine. Ar=3,5-dimethylphenyl, BINAP=2,2′-bis(diphenylphosphanyl)-1,1′-binaphthyl, BIPHEP=2,2′-bis(diarylphosphanyl)biphenyl.
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DOI:
10.1002/(SICI)1521-3773(19990215)38:43.0.CO;2-O
被引量:
年份:
1999
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