C-2-symmetric bisphosphine ligands derived from 1,1 '-binaphthyldiamines and diphenylphosphinobenzoic acid for palladium catalyzed desymmetrizations

Authors
Lim, CWLee, S
Issue Date
2000-07-14
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
TETRAHEDRON, v.56, no.29, pp.5131 - 5136
Abstract
A series of novel C-2-symmetric bisphosphine ligands derived from DPPBA and C-2-symmetric 1,1'-binaphthyldiamines has been synthesized. In palladium catalyzed desymmetrization of meso cyclic carbamates, the enantioselectivity and the stereochemistry of the major enantiomers are largely affected by the substitution position of DPPBA moiety on the 1,1'-binaphthyl chiral scaffold. (C) 2000 Elsevier Science Ltd. All rights reserved.
Keywords
ASYMMETRIC ALLYLIC SUBSTITUTION; CYCLIC BORATE ESTER; BINAPHTHOL DERIVATIVES; ARYL BROMIDES; ENANTIOSELECTIVE SYNTHESIS; REDUCTIVE ELIMINATION; MOLECULAR RECOGNITION; COUPLING REACTIONS; SECONDARY-AMINES; FACILE SYNTHESIS; ASYMMETRIC ALLYLIC SUBSTITUTION; CYCLIC BORATE ESTER; BINAPHTHOL DERIVATIVES; ARYL BROMIDES; ENANTIOSELECTIVE SYNTHESIS; REDUCTIVE ELIMINATION; MOLECULAR RECOGNITION; COUPLING REACTIONS; SECONDARY-AMINES; FACILE SYNTHESIS; C-2-symmetric; binaphthylbisphosphine; palladium; desymmetrizations
ISSN
0040-4020
URI
https://pubs.kist.re.kr/handle/201004/141231
DOI
10.1016/S0040-4020(00)00420-8
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KIST Article > 2000
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