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2-diphenylphosphino-2'-diphenylphosphinyl-1,1'-binaphthalene (BINAPO), an axially chiral heterobidentate ligand for enantioselective catalysis

Academic Article
Publication Date:
1998
abstract:
Racemic 2-diphenylphosphino-2'-diphenylphosphinyl-1,1'-binaphthalene (BINAPO) 5 has been prepared in four steps from 1,1'-binaphthalene-2,2'-diol (BINOL) 1 and has been resolved with the aid of the C,N-cyclopalladated complex with N,N-dimethyl (S)-1-(1-naphthyl)ethylamine 6. P,O-chelate binding to palladium occurs in solution and this is confirmed in the solid state by X-ray analysis. (S)-BINAPO is an immediate precursor of (S)-BINAP and is itself an effective chiral inducer for the Pd-catalyzed asymmetric hydrosilylation of styrene (over 70% e.e.).
Iris type:
01.01 Articolo in rivista
Keywords:
BINAPO; asymmetric hydrosilylation
List of contributors:
Fabbri, DAVIDE GAETANO
Authors of the University:
FABBRI DAVIDE GAETANO
Handle:
https://iris.cnr.it/handle/20.500.14243/390002
Published in:
TETRAHEDRON-ASYMMETRY
Journal
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http://www.scopus.com/record/display.url?eid=2-s2.0-0032512598&origin=inward
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