A diacetate ketone-catalyzed asymmetric epoxidation of olefins

Bin Wang; Xin Yan Wu; O. Andrea Wong; Brian Nettles; Mei Xin Zhao; Dajun Chen; Yian Shi

doi:10.1021/jo900330n

A diacetate ketone-catalyzed asymmetric epoxidation of olefins

Bin Wang, Xin Yan Wu, O. Andrea Wong, Brian Nettles, Mei Xin Zhao, Dajun Chen, Yian Shi

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

52 Scopus citations

Abstract

(Chemical Equation Presented) A fructose-derived diacetate ketone has been shown to be an effective catalyst for asymmetric epoxidation. High ee values have been obtained for a variety of trans and trisubstituted olefins including electron-deficient α,β-unsaturated esters as well as certain cis olefins.

Original language	English (US)
Pages (from-to)	3986-3989
Number of pages	4
Journal	Journal of Organic Chemistry
Volume	74
Issue number	10
DOIs	https://doi.org/10.1021/jo900330n
State	Published - May 15 2009
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry

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10.1021/jo900330n

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title = "A diacetate ketone-catalyzed asymmetric epoxidation of olefins",

abstract = "(Chemical Equation Presented) A fructose-derived diacetate ketone has been shown to be an effective catalyst for asymmetric epoxidation. High ee values have been obtained for a variety of trans and trisubstituted olefins including electron-deficient α,β-unsaturated esters as well as certain cis olefins.",

author = "Bin Wang and Wu, {Xin Yan} and Wong, {O. Andrea} and Brian Nettles and Zhao, {Mei Xin} and Dajun Chen and Yian Shi",

year = "2009",

month = may,

day = "15",

doi = "10.1021/jo900330n",

language = "English (US)",

volume = "74",

pages = "3986--3989",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

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T1 - A diacetate ketone-catalyzed asymmetric epoxidation of olefins

AU - Wang, Bin

AU - Wu, Xin Yan

AU - Wong, O. Andrea

AU - Nettles, Brian

AU - Zhao, Mei Xin

AU - Chen, Dajun

AU - Shi, Yian

PY - 2009/5/15

Y1 - 2009/5/15

N2 - (Chemical Equation Presented) A fructose-derived diacetate ketone has been shown to be an effective catalyst for asymmetric epoxidation. High ee values have been obtained for a variety of trans and trisubstituted olefins including electron-deficient α,β-unsaturated esters as well as certain cis olefins.

AB - (Chemical Equation Presented) A fructose-derived diacetate ketone has been shown to be an effective catalyst for asymmetric epoxidation. High ee values have been obtained for a variety of trans and trisubstituted olefins including electron-deficient α,β-unsaturated esters as well as certain cis olefins.

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U2 - 10.1021/jo900330n

DO - 10.1021/jo900330n

M3 - Article

C2 - 19388627

AN - SCOPUS:65949109033

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EP - 3989

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 10

ER -

A diacetate ketone-catalyzed asymmetric epoxidation of olefins

Abstract

ASJC Scopus subject areas

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