123675-57-0Relevant articles and documents
C2-symmetric bisphosphine ligands derived from 1,1- binaphthyldiamines and diphenylphosphinobenzoic acid for palladium catalyzed desymmetrizations
Lim, Chung Woo,Lee, Sang-gi
, p. 5131 - 5136 (2000)
A series of novel C2-symmetric bisphosphine ligands derived from DPPBA and C2-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.
Chiral Recognition in Clefts and Cyclophane Cavities Shaped by the 1,1'-Binaphthyl Major Groove
Castro, Peter P.,Georgiadis, Taxiarchis M.,Diederich, Francois
, p. 5835 - 5838 (1989)
The optical resolution of 7,7'-bis(benzyloxy)-2,2'-dihydroxy-1,1'-binaphthyl through clathrate formation with quinine is described.Optically active cyclophanes incorporating this spacer bind enantioselectively naproxen derivatives.Hydrogen bonding and ?-?
Optically active diphosphine, transition metal complex containing the same, and process for producing optically active compound using the complex
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, (2008/06/13)
Disclosed are an optically active diphosphine represented by formula: STR1 wherein R represents a lower alkyl group having 1 to 4 carbon atoms; Ar represents a phenyl group which may be substituted with a lower alkyl group having 1 to 4 carbon atoms and/o
Synthesis of (R)- and (S)-7,7'-Bis(diphenylphosphino)-2,2'-dimethoxy-1,1'-binaphthyl, a New Axially Dissymmetric Bis(triarylphosphine)
Horiuchi, Toshihide,Ohta, Tetsuo,Stephan, Massoud,Takaya, Hidemasa
, p. 325 - 328 (2007/10/02)
A new axially dissymmetric bis(triarylphosphine) ligand 7,7'-bis(diphenylphosphino)-2,2'-dimethoxy-1,1'-binaphthyl has been synthesized in enantiomerically pure form.
Chiral recognition of cinchona alkaloids at the minor and major grooves of 1,1'-binaphthyl receptors
Reeder,Castro,Knobler,Martinborough,Owens,Diederich
, p. 3151 - 3160 (2007/10/02)
A variety of chiral 1,1'-binaphthyl derivatives with one or two hydroxyl groups at either the 2,2'-(minor groove) or the 7,7'-positions (major groove) were prepared for enantioselective recognition of the cinchona alkaloids quinine and quinidine. The stud