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

31 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
Externally published	Yes

ASJC Scopus subject areas

Molecular Medicine

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10.1039/C39930000327

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

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.",

author = "Masahiro Terada and Satoru Matsukawa and Koichi Mikami",

year = "1993",

doi = "10.1039/C39930000327",

language = "English",

pages = "327--328",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "3",

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T1 - Enantiomerically pure compound synthesis by asymmetric glyoxylate-ene reaction with vinylic sulfides and selenides catalysed by a chiral titanium complex

AU - Terada, Masahiro

AU - Matsukawa, Satoru

AU - Mikami, Koichi

PY - 1993

Y1 - 1993

N2 - 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.

AB - 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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DO - 10.1039/C39930000327

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EP - 328

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 3

ER -

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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