Enantiomerically pure compound synthesis by asymmetric glyoxylate-ene reaction with vinylic sulfides and selenides catalysed by a chiral titanium complex

Masahiro Terada; Satoru Matsukawa; Koichi Mikami

doi:10.1039/C39930000327

Enantiomerically pure compound synthesis by asymmetric glyoxylate-ene reaction with vinylic sulfides and selenides catalysed by a chiral titanium complex

Masahiro Terada, Satoru Matsukawa, Koichi Mikami

Research output: Contribution to journal › Article › peer-review

30 Citations (Scopus)

Abstract

Asymmetric catalysis of the glyoxylate-ene reaction with vinylic sulfides and selenides by a binaphthol-derived titanium complex provides enantiomerically pure (e.p.) diastereoisomers (anti and Z) of β-alkyl-α-hydroxy esters.

Original language	English
Pages (from-to)	327-328
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	3
DOIs	https://doi.org/10.1039/C39930000327
Publication status	Published - 1993 Dec 1
Externally published	Yes

ASJC Scopus subject areas

Molecular Medicine

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Enantiomerically pure compound synthesis by asymmetric glyoxylate-ene reaction with vinylic sulfides and selenides catalysed by a chiral titanium complex. / Terada, Masahiro; Matsukawa, Satoru; Mikami, Koichi.

In: Journal of the Chemical Society, Chemical Communications, No. 3, 01.12.1993, p. 327-328.

Research output: Contribution to journal › Article › peer-review

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abstract = "Asymmetric catalysis of the glyoxylate-ene reaction with vinylic sulfides and selenides by a binaphthol-derived titanium complex provides enantiomerically pure (e.p.) diastereoisomers (anti and Z) of β-alkyl-α-hydroxy esters.",

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Enantiomerically pure compound synthesis by asymmetric glyoxylate-ene reaction with vinylic sulfides and selenides catalysed by a chiral titanium complex

Abstract

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