Fluoride catalyzed Michael reaction of α-isocyanoesters with α,β-unsaturated carbonyl compounds

Masahiro Murakami; Naoki Hasegawa; Ikuyoshi Tomita; Masahiko Inouye; Yoshihiko Ito

doi:10.1016/S0040-4039(00)72729-8

Fluoride catalyzed Michael reaction of α-isocyanoesters with α,β-unsaturated carbonyl compounds

Masahiro Murakami^*, Naoki Hasegawa, Ikuyoshi Tomita, Masahiko Inouye, Yoshihiko Ito

^*Corresponding author for this work

Member of the Board

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

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Abstract

The Michael reaction of α-isocyanoesters with α,β-unsaturated carbonyl compounds was efficiently promoted by a catalytic amount of tetrabutylammonium fluoride to produce α-isocyano-δ-ketoesters or silyl ethers of their enols in high yields.

Original language	English
Pages (from-to)	1257-1260
Number of pages	4
Journal	Tetrahedron Letters
Volume	30
Issue number	10
DOIs	https://doi.org/10.1016/S0040-4039(00)72729-8
State	Published - 1989

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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@article{25853a605a7440cfb07a67fd0247fda9,

title = "Fluoride catalyzed Michael reaction of α-isocyanoesters with α,β-unsaturated carbonyl compounds",

abstract = "The Michael reaction of α-isocyanoesters with α,β-unsaturated carbonyl compounds was efficiently promoted by a catalytic amount of tetrabutylammonium fluoride to produce α-isocyano-δ-ketoesters or silyl ethers of their enols in high yields.",

author = "Masahiro Murakami and Naoki Hasegawa and Ikuyoshi Tomita and Masahiko Inouye and Yoshihiko Ito",

year = "1989",

doi = "10.1016/S0040-4039(00)72729-8",

language = "英語",

volume = "30",

pages = "1257--1260",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd.",

number = "10",

}

TY - JOUR

T1 - Fluoride catalyzed Michael reaction of α-isocyanoesters with α,β-unsaturated carbonyl compounds

AU - Murakami, Masahiro

AU - Hasegawa, Naoki

AU - Tomita, Ikuyoshi

AU - Inouye, Masahiko

AU - Ito, Yoshihiko

PY - 1989

Y1 - 1989

N2 - The Michael reaction of α-isocyanoesters with α,β-unsaturated carbonyl compounds was efficiently promoted by a catalytic amount of tetrabutylammonium fluoride to produce α-isocyano-δ-ketoesters or silyl ethers of their enols in high yields.

AB - The Michael reaction of α-isocyanoesters with α,β-unsaturated carbonyl compounds was efficiently promoted by a catalytic amount of tetrabutylammonium fluoride to produce α-isocyano-δ-ketoesters or silyl ethers of their enols in high yields.

UR - http://www.scopus.com/inward/record.url?scp=0342333699&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)72729-8

DO - 10.1016/S0040-4039(00)72729-8

M3 - 学術論文

AN - SCOPUS:0342333699

SN - 0040-4039

VL - 30

SP - 1257

EP - 1260

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 10

ER -

Fluoride catalyzed Michael reaction of α-isocyanoesters with α,β-unsaturated carbonyl compounds

Abstract

ASJC Scopus subject areas

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