[Synthesis and properties of optically active organoantimony compounds]

Yasuike, S

HERO ID

1022206

Reference Type

Journal Article

Subtype

Review

Year

2003

Language

Japanese

PMID

12875240

HERO ID 1022206
Material Type Review
In Press No
Year 2003
Title [Synthesis and properties of optically active organoantimony compounds]
Authors Yasuike, S
Journal Yakugaku Zasshi
Volume 123
Issue 7
Page Numbers 577-585
Abstract The chemistry of chiral ligands for transition metal-catalyzed asymmetric reactions is an interesting research field in synthetic chemistry and has recently been the focus of much attention. Although a number of chiral ligands containing phosphorus (P) and arsenic (As) have been widely studied and are well documented, asymmetric reactions with optically active organoantimony compounds have not been reported so far. We are interested in the synthesis and utilization of optically active organoantimony compounds for asymmetric synthesis. We present here the synthesis and resolution of Sb-chiral and C2-symmetric compounds containing antimony as well as their physical and chemical properties. Resolution of (+/-)-1-phenyl-2-trimetylsilylstibindole (1), Sb (R/S)-(aryl) [2-(S)-(1-dimethylaminoethyl) phenyl] (p-tolyl) stibane (9), and (+/-)-2,2'-bis(diarylstibano)-1,1'-binaphthyl (13) can be achieved by the separation of a mixture of the diastereomeric antimony-palladium complexes. The optically pure Sb-chiral stibanes (1, 9) isolated here were optically stable, and no racemization on the chiral antimony center was observed even when they were heated under a neutral or a basic condition. Single-crystal X-ray analysis of Sb-chiral triarylstibane 9b-B revealed the presence of an intramolecular interaction between the antimony and nitrogen atoms. The optically active BINASb (13) can be used as powerful chiral ligand for the palladium-catalyzed asymmetric allylic alkylation of racemic 1,3-diphenyl-2-propen-1-yl acetate with dimethyl malonate. We also report the synthesis, molecular structure, and fluxional behavior of the (R)-(-)-7-p-tolyl-dinaphtho [2, 1-b; 1',2'-d] stibole (21c) which is the first isolated example of optically active C2-symmetric group 15 dinaphthoheteroles.
Pmid 12875240
Wosid WOS:000183949800008
Is Certified Translation No
Dupe Override No
Comments |WOS:000183949800008
Is Public Yes
Language Text Japanese
Keyword optically active organoantimony; Sb-chiral; BINASb; diastereomeric palladium complex; dinaphthoheterole; fluxional behavior
Is Qa No