Addition-elimination strategy for asymmetric induction: A chiral sulfoxide as a leaving group

Kaoru Fuji; Manabu Node; Hitoshi Abe; Akichika Itoh; Yukio Masaki; Motoo Shiro

doi:10.1016/S0040-4039(00)97377-5

Addition-elimination strategy for asymmetric induction: A chiral sulfoxide as a leaving group

Kaoru Fuji^*, Manabu Node, Hitoshi Abe, Akichika Itoh, Yukio Masaki, Motoo Shiro

^*Corresponding author for this work

Applied Chemistry

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

25 Scopus citations

Abstract

The reaction of β-nitro-α,β-unsaturated sulfoxide 7 with δ-lactam enolates 11 - 15 afforded 20 - 24, respectively, in good chemical yields with high enantiomeric excesses.

Original language	English
Pages (from-to)	2419-2422
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	17
DOIs	https://doi.org/10.1016/S0040-4039(00)97377-5
State	Published - 1990

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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@article{df21501660194c17b6f194f8b630e70d,

title = "Addition-elimination strategy for asymmetric induction: A chiral sulfoxide as a leaving group",

abstract = "The reaction of β-nitro-α,β-unsaturated sulfoxide 7 with δ-lactam enolates 11 - 15 afforded 20 - 24, respectively, in good chemical yields with high enantiomeric excesses.",

author = "Kaoru Fuji and Manabu Node and Hitoshi Abe and Akichika Itoh and Yukio Masaki and Motoo Shiro",

year = "1990",

doi = "10.1016/S0040-4039(00)97377-5",

language = "英語",

volume = "31",

pages = "2419--2422",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd.",

number = "17",

}

TY - JOUR

T1 - Addition-elimination strategy for asymmetric induction

T2 - A chiral sulfoxide as a leaving group

AU - Fuji, Kaoru

AU - Node, Manabu

AU - Abe, Hitoshi

AU - Itoh, Akichika

AU - Masaki, Yukio

AU - Shiro, Motoo

PY - 1990

Y1 - 1990

N2 - The reaction of β-nitro-α,β-unsaturated sulfoxide 7 with δ-lactam enolates 11 - 15 afforded 20 - 24, respectively, in good chemical yields with high enantiomeric excesses.

AB - The reaction of β-nitro-α,β-unsaturated sulfoxide 7 with δ-lactam enolates 11 - 15 afforded 20 - 24, respectively, in good chemical yields with high enantiomeric excesses.

UR - http://www.scopus.com/inward/record.url?scp=0025253531&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)97377-5

DO - 10.1016/S0040-4039(00)97377-5

M3 - 学術論文

AN - SCOPUS:0025253531

SN - 0040-4039

VL - 31

SP - 2419

EP - 2422

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 17

ER -

Addition-elimination strategy for asymmetric induction: A chiral sulfoxide as a leaving group

Abstract

ASJC Scopus subject areas

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