A convenient high yielding synthesis of nor-alcohols from carboxylic acids

Derek H.R. Barton; Dominique Bridon; Samir Z. Zard

doi:10.1039/c39850001066

A convenient high yielding synthesis of nor-alcohols from carboxylic acids

Derek H.R. Barton
, Dominique Bridon
, Samir Z. Zard

Institut de Chimie des Substances Naturelles

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

43 Citations (Scopus)

Abstract

Esters (mixed anhydrides) of carboxylic acids and thiohydroxamic acid (2) react with tris(phenylthio)antimony in the presence of oxygen and water to give high yields of nor-alcohols.

Original language	English
Pages (from-to)	1066-1068
Number of pages	3
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	16
DOIs	https://doi.org/10.1039/c39850001066
Publication status	Published - 1 Jan 1985
Externally published	Yes

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title = "A convenient high yielding synthesis of nor-alcohols from carboxylic acids",

abstract = "Esters (mixed anhydrides) of carboxylic acids and thiohydroxamic acid (2) react with tris(phenylthio)antimony in the presence of oxygen and water to give high yields of nor-alcohols.",

author = "Barton, \{Derek H.R.\} and Dominique Bridon and Zard, \{Samir Z.\}",

year = "1985",

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language = "English",

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journal = "Journal of the Chemical Society, Chemical Communications",

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AU - Barton, Derek H.R.

AU - Bridon, Dominique

AU - Zard, Samir Z.

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N2 - Esters (mixed anhydrides) of carboxylic acids and thiohydroxamic acid (2) react with tris(phenylthio)antimony in the presence of oxygen and water to give high yields of nor-alcohols.

AB - Esters (mixed anhydrides) of carboxylic acids and thiohydroxamic acid (2) react with tris(phenylthio)antimony in the presence of oxygen and water to give high yields of nor-alcohols.

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DO - 10.1039/c39850001066

M3 - Article

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SP - 1066

EP - 1068

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 16

ER -

A convenient high yielding synthesis of nor-alcohols from carboxylic acids

Abstract

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