Direct epoxidation of unprotected olefinic carboxylic acids using HOF-CH3CN

Shlomo Rozen; Yifat Bareket; Sharon Dayan

doi:10.1016/0040-4039(95)02180-9

Direct epoxidation of unprotected olefinic carboxylic acids using HOF-CH₃CN

Shlomo Rozen^*, Yifat Bareket, Sharon Dayan

^*Corresponding author for this work

School of Chemistry

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

Abstract

The reaction of HOF·CH₃CN complex, made directly by passing fluorine through aqueous acetonitrile, with double bond containing unprotected carboxylic acids and alcohols results in fast and almost quantitative epoxidation.

Original language	English
Pages (from-to)	531-534
Number of pages	4
Journal	Tetrahedron Letters
Volume	37
Issue number	4
DOIs	https://doi.org/10.1016/0040-4039(95)02180-9
State	Published - 22 Jan 1996

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@article{e55dce22c14b4b4fa0224c70d7a19e31,

title = "Direct epoxidation of unprotected olefinic carboxylic acids using HOF-CH3CN",

abstract = "The reaction of HOF·CH3CN complex, made directly by passing fluorine through aqueous acetonitrile, with double bond containing unprotected carboxylic acids and alcohols results in fast and almost quantitative epoxidation.",

author = "Shlomo Rozen and Yifat Bareket and Sharon Dayan",

year = "1996",

month = jan,

day = "22",

doi = "10.1016/0040-4039(95)02180-9",

language = "אנגלית",

volume = "37",

pages = "531--534",

journal = "Tetrahedron Letters",

issn = "0040-4039",

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number = "4",

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TY - JOUR

T1 - Direct epoxidation of unprotected olefinic carboxylic acids using HOF-CH3CN

AU - Rozen, Shlomo

AU - Bareket, Yifat

AU - Dayan, Sharon

PY - 1996/1/22

Y1 - 1996/1/22

N2 - The reaction of HOF·CH3CN complex, made directly by passing fluorine through aqueous acetonitrile, with double bond containing unprotected carboxylic acids and alcohols results in fast and almost quantitative epoxidation.

AB - The reaction of HOF·CH3CN complex, made directly by passing fluorine through aqueous acetonitrile, with double bond containing unprotected carboxylic acids and alcohols results in fast and almost quantitative epoxidation.

UR - http://www.scopus.com/inward/record.url?scp=0030033654&partnerID=8YFLogxK

U2 - 10.1016/0040-4039(95)02180-9

DO - 10.1016/0040-4039(95)02180-9

M3 - מאמר

AN - SCOPUS:0030033654

VL - 37

SP - 531

EP - 534

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 4

ER -

Direct epoxidation of unprotected olefinic carboxylic acids using HOF-CH₃CN

Abstract

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