Radical reactions in esters with alkoxy functionality chemistry an unusual alcohol moiety hydrogen abstraction

Ming Chung Yan; Yeong Jiunn Jang; Jhenyi Wu; Yung Feng Lin; Ching Fa Yao

doi:10.1016/j.tetlet.2004.02.158

Radical reactions in esters with alkoxy functionality chemistry an unusual alcohol moiety hydrogen abstraction

Ming Chung Yan
, Yeong Jiunn Jang
, Jhenyi Wu
, Yung Feng Lin
, Ching Fa Yao^*

^*Corresponding author for this work

Department of Chemistry

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

9 Citations (Scopus)

Abstract

Various geometrically pure (E)-alkenes have been synthesized by radical substitution of alcohol moieties generated via hydrogen abstraction within ethyl esters. These reactions occurred with high regioselectivity and gave a new access to 1-methyl-3-aryl-allyl esters.

Original language	English
Pages (from-to)	3685-3687
Number of pages	3
Journal	Tetrahedron Letters
Volume	45
Issue number	18
DOIs	https://doi.org/10.1016/j.tetlet.2004.02.158
Publication status	Published - 2004 Apr 26

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2004.02.158

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title = "Radical reactions in esters with alkoxy functionality chemistry an unusual alcohol moiety hydrogen abstraction",

abstract = "Various geometrically pure (E)-alkenes have been synthesized by radical substitution of alcohol moieties generated via hydrogen abstraction within ethyl esters. These reactions occurred with high regioselectivity and gave a new access to 1-methyl-3-aryl-allyl esters.",

author = "Yan, \{Ming Chung\} and Jang, \{Yeong Jiunn\} and Jhenyi Wu and Lin, \{Yung Feng\} and Yao, \{Ching Fa\}",

note = "Funding Information: Financial support of this work by the National Science Council of the Republic of China is gratefully acknowledged. ",

year = "2004",

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doi = "10.1016/j.tetlet.2004.02.158",

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journal = "Tetrahedron Letters",

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T1 - Radical reactions in esters with alkoxy functionality chemistry an unusual alcohol moiety hydrogen abstraction

AU - Yan, Ming Chung

AU - Jang, Yeong Jiunn

AU - Wu, Jhenyi

AU - Lin, Yung Feng

AU - Yao, Ching Fa

N1 - Funding Information: Financial support of this work by the National Science Council of the Republic of China is gratefully acknowledged.

PY - 2004/4/26

Y1 - 2004/4/26

N2 - Various geometrically pure (E)-alkenes have been synthesized by radical substitution of alcohol moieties generated via hydrogen abstraction within ethyl esters. These reactions occurred with high regioselectivity and gave a new access to 1-methyl-3-aryl-allyl esters.

AB - Various geometrically pure (E)-alkenes have been synthesized by radical substitution of alcohol moieties generated via hydrogen abstraction within ethyl esters. These reactions occurred with high regioselectivity and gave a new access to 1-methyl-3-aryl-allyl esters.

UR - https://www.scopus.com/pages/publications/1842736534

UR - https://www.scopus.com/pages/publications/1842736534#tab=citedBy

U2 - 10.1016/j.tetlet.2004.02.158

DO - 10.1016/j.tetlet.2004.02.158

M3 - Article

AN - SCOPUS:1842736534

SN - 0040-4039

VL - 45

SP - 3685

EP - 3687

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 18

ER -

Radical reactions in esters with alkoxy functionality chemistry an unusual alcohol moiety hydrogen abstraction

Abstract

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