One-step synthesis of α,β-unsaturated ketones by the reaction of enol acetates with allyl methyl carbonate catalyzed by palladium and tin compounds

Jiro Tsuji; Ichiro Minami; Isao Shimizu

doi:10.1016/S0040-4039(00)94161-3

One-step synthesis of α,β-unsaturated ketones by the reaction of enol acetates with allyl methyl carbonate catalyzed by palladium and tin compounds

Jiro Tsuji^*, Ichiro Minami, Isao Shimizu

^*Corresponding author for this work

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

38 Citations (Scopus)

Abstract

Enol acetates derived from saturated ketones are converted to α,β-unsaturated ketones by heating with allyl methyl carbonate in MeCN by bimetallic catalysis of palladium-phosphine complex and tin methoxide.

Original language	English
Pages (from-to)	5639-5640
Number of pages	2
Journal	Tetrahedron Letters
Volume	24
Issue number	50
DOIs	https://doi.org/10.1016/S0040-4039(00)94161-3
Publication status	Published - 1983

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

Access to Document

10.1016/S0040-4039(00)94161-3

Cite this

@article{e683ea9d2cfc4379b2cceea217c8d439,

title = "One-step synthesis of α,β-unsaturated ketones by the reaction of enol acetates with allyl methyl carbonate catalyzed by palladium and tin compounds",

abstract = "Enol acetates derived from saturated ketones are converted to α,β-unsaturated ketones by heating with allyl methyl carbonate in MeCN by bimetallic catalysis of palladium-phosphine complex and tin methoxide.",

author = "Jiro Tsuji and Ichiro Minami and Isao Shimizu",

year = "1983",

doi = "10.1016/S0040-4039(00)94161-3",

language = "English",

volume = "24",

pages = "5639--5640",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "50",

}

TY - JOUR

T1 - One-step synthesis of α,β-unsaturated ketones by the reaction of enol acetates with allyl methyl carbonate catalyzed by palladium and tin compounds

AU - Tsuji, Jiro

AU - Minami, Ichiro

AU - Shimizu, Isao

PY - 1983

Y1 - 1983

N2 - Enol acetates derived from saturated ketones are converted to α,β-unsaturated ketones by heating with allyl methyl carbonate in MeCN by bimetallic catalysis of palladium-phosphine complex and tin methoxide.

AB - Enol acetates derived from saturated ketones are converted to α,β-unsaturated ketones by heating with allyl methyl carbonate in MeCN by bimetallic catalysis of palladium-phosphine complex and tin methoxide.

UR - http://www.scopus.com/inward/record.url?scp=0000895752&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0000895752&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)94161-3

DO - 10.1016/S0040-4039(00)94161-3

M3 - Article

AN - SCOPUS:0000895752

SN - 0040-4039

VL - 24

SP - 5639

EP - 5640

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 50

ER -

One-step synthesis of α,β-unsaturated ketones by the reaction of enol acetates with allyl methyl carbonate catalyzed by palladium and tin compounds

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this