A new C-3-symmetric chiral bisphosphine ligand containing a bioxazole backbone: highly enantioselective hydrosilylation of ketones

Authors
Lee, SGLim, CWSong, CEKim, IO
Issue Date
1997-12-23
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON-ASYMMETRY, v.8, no.24, pp.4027 - 4031
Abstract
C-2-Symmetric (4S,4'S)-2,2'-bis(o-diphenylphosphinophenyl)-4,4',5,5'- tetrahydro-4,4'-bi(1,3-oxazole) (1, Phos-Bidx) has been designed and synthesized as a chiral ligand for metal-catalyzed reactions. The Phos-Biox 1 was found to be an efficient ligand for rhodium(I)-catalyzed asymmetric reduction of prochiral acetophenones with diphenylsilane to give optically active secondary alcohols of up to 97% ee. (C) 1997 Elsevier Science Ltd. All rights reserved.
Keywords
CATALYZED ASYMMETRIC HYDROSILYLATION; CONTAINING OXAZOLINE LIGANDS; PHOSPHINE HYBRID LIGAND; ALLYLIC SUBSTITUTION; CYCLOPROPANATION; COMPLEXES; HYDROGENATION; OLEFINS; DERIVATIVES; ALKYLATIONS; CATALYZED ASYMMETRIC HYDROSILYLATION; CONTAINING OXAZOLINE LIGANDS; PHOSPHINE HYBRID LIGAND; ALLYLIC SUBSTITUTION; CYCLOPROPANATION; COMPLEXES; HYDROGENATION; OLEFINS; DERIVATIVES; ALKYLATIONS; C//2-symmetric bioxazole ligand
ISSN
0957-4166
URI
https://pubs.kist.re.kr/handle/201004/143450
DOI
10.1016/S0957-4166(97)00554-5
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