Facile and regioselective synthesis of phenylpropanoid-substituted flavan-3-ols

Suresh Awale; Yasuhiro Tezuka; Shumin Wang; Shigetoshi Kadota

doi:10.1021/ol020042n

Facile and regioselective synthesis of phenylpropanoid-substituted flavan-3-ols

Suresh Awale, Yasuhiro Tezuka, Shumin Wang, Shigetoshi Kadota^*

^*Corresponding author for this work

Section of Natural Products & Drug Discovery, Division of Medicinal Resources, Institute of Natural Medicine

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

20 Scopus citations

Abstract

Matrix presented A highly efficient, facile, one-pot regioselective synthesis of a series of phenylpropanoid-substituted flavan-3-ols is described. The mechanism involves dienone-phenol rearrangement followed by a Michael-type reaction.

Original language	English
Pages (from-to)	1707-1709
Number of pages	3
Journal	Organic Letters
Volume	4
Issue number	10
DOIs	https://doi.org/10.1021/ol020042n
State	Published - 2002/05/16

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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@article{206ec81215fd4136bf6b6fad804ab66f,

title = "Facile and regioselective synthesis of phenylpropanoid-substituted flavan-3-ols",

abstract = "Matrix presented A highly efficient, facile, one-pot regioselective synthesis of a series of phenylpropanoid-substituted flavan-3-ols is described. The mechanism involves dienone-phenol rearrangement followed by a Michael-type reaction.",

author = "Suresh Awale and Yasuhiro Tezuka and Shumin Wang and Shigetoshi Kadota",

year = "2002",

month = may,

day = "16",

doi = "10.1021/ol020042n",

language = "英語",

volume = "4",

pages = "1707--1709",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "10",

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TY - JOUR

T1 - Facile and regioselective synthesis of phenylpropanoid-substituted flavan-3-ols

AU - Awale, Suresh

AU - Tezuka, Yasuhiro

AU - Wang, Shumin

AU - Kadota, Shigetoshi

PY - 2002/5/16

Y1 - 2002/5/16

N2 - Matrix presented A highly efficient, facile, one-pot regioselective synthesis of a series of phenylpropanoid-substituted flavan-3-ols is described. The mechanism involves dienone-phenol rearrangement followed by a Michael-type reaction.

AB - Matrix presented A highly efficient, facile, one-pot regioselective synthesis of a series of phenylpropanoid-substituted flavan-3-ols is described. The mechanism involves dienone-phenol rearrangement followed by a Michael-type reaction.

UR - http://www.scopus.com/inward/record.url?scp=0037118325&partnerID=8YFLogxK

U2 - 10.1021/ol020042n

DO - 10.1021/ol020042n

M3 - 学術論文

C2 - 12000279

AN - SCOPUS:0037118325

SN - 1523-7060

VL - 4

SP - 1707

EP - 1709

JO - Organic Letters

JF - Organic Letters

IS - 10

ER -

Facile and regioselective synthesis of phenylpropanoid-substituted flavan-3-ols

Abstract

ASJC Scopus subject areas

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