Issue 3, 2000

Resolution of racemic Sb-chiral stibindoles using an optically active ortho-palladated benzylamine derivative, via their diastereomeric complexes

Abstract

Resolution of racemic Sb-chiral (±)-1-phenyl-2-trimethylsilylstibindole 1 has been achieved by the separation of a mixture of the diastereomeric palladium(II) complexes 3A and 3B derived from the reaction of (±)-1 with di-μ-chlorobis{(S)-2-[1-(dimethylamino)ethyl]phenyl-C ,N}dipalladium(II) 2, and optically pure 1-phenylstibindoles (-)-4 and (+)-4 have also been obtained from resolved (−)-1 and (+)-1, respectively.

Article information

Article type
Communication
Submitted
22 Nov 1999
Accepted
17 Dec 1999
First published
26 Jan 2000

Chem. Commun., 2000, 191-192

Resolution of racemic Sb-chiral stibindoles using an optically active ortho-palladated benzylamine derivative, via their diastereomeric complexes

J. Kurita, F. Usuda, S. Yasuike, T. Tsuchiya, Y. Tsuda, F. Kiuchi and S. Hosoi, Chem. Commun., 2000, 191 DOI: 10.1039/A909200E

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