Palladium-catalyzed allylation of ketones and aldehydes via allyl enol carbonates

Jiro Tsuji; Ichiro Minami; Isao Shimizu

doi:10.1016/S0040-4039(00)81772-4

Palladium-catalyzed allylation of ketones and aldehydes via allyl enol carbonates

Jiro Tsuji^*, Ichiro Minami, Isao Shimizu

^*Corresponding author for this work

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

118 Citations (Scopus)

Abstract

Rearrangement of allyl enol carbonates, prepared from ketones or aldehydes by trapping their enolates with allyl chloroformate, to give α-allyl ketones or aldehydes regioselectivity is catalyzed by palladium-phosphine complexes under mild conditions.

Original language	English
Pages (from-to)	1793-1796
Number of pages	4
Journal	Tetrahedron Letters
Volume	24
Issue number	17
DOIs	https://doi.org/10.1016/S0040-4039(00)81772-4
Publication status	Published - 1983

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

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10.1016/S0040-4039(00)81772-4

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@article{05156d60cc50460caf163aec71e2d290,

title = "Palladium-catalyzed allylation of ketones and aldehydes via allyl enol carbonates",

abstract = "Rearrangement of allyl enol carbonates, prepared from ketones or aldehydes by trapping their enolates with allyl chloroformate, to give α-allyl ketones or aldehydes regioselectivity is catalyzed by palladium-phosphine complexes under mild conditions.",

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

year = "1983",

doi = "10.1016/S0040-4039(00)81772-4",

language = "English",

volume = "24",

pages = "1793--1796",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "17",

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TY - JOUR

T1 - Palladium-catalyzed allylation of ketones and aldehydes via allyl enol carbonates

AU - Tsuji, Jiro

AU - Minami, Ichiro

AU - Shimizu, Isao

PY - 1983

Y1 - 1983

N2 - Rearrangement of allyl enol carbonates, prepared from ketones or aldehydes by trapping their enolates with allyl chloroformate, to give α-allyl ketones or aldehydes regioselectivity is catalyzed by palladium-phosphine complexes under mild conditions.

AB - Rearrangement of allyl enol carbonates, prepared from ketones or aldehydes by trapping their enolates with allyl chloroformate, to give α-allyl ketones or aldehydes regioselectivity is catalyzed by palladium-phosphine complexes under mild conditions.

UR - http://www.scopus.com/inward/record.url?scp=0001279801&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0001279801&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)81772-4

DO - 10.1016/S0040-4039(00)81772-4

M3 - Article

AN - SCOPUS:0001279801

SN - 0040-4039

VL - 24

SP - 1793

EP - 1796

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 17

ER -

Palladium-catalyzed allylation of ketones and aldehydes via allyl enol carbonates

Abstract

ASJC Scopus subject areas

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