A Mild and Convenient Oxidation Procedure for the Conversion of Organoboranes to the Corresponding Alcohols

George Kabalka, Herbert C. Hedgecock

Research output: Contribution to journalArticle

97 Citations (Scopus)

Abstract

Organoboranes are oxidized efficiently by trimethylamine N-oxide dihydrate. The reagent is exceptionally mild, permitting the oxidation of a wide variety of functionally substituted organoboranes. In every instance the yields of product alcohol are as good as or better than the yields obtained using the standard oxidation procedure.

Original languageEnglish (US)
Pages (from-to)1776-1779
Number of pages4
JournalJournal of Organic Chemistry
Volume40
Issue number12
DOIs
StatePublished - Jun 1 1975

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Alcohols
Oxidation
trimethyloxamine

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

A Mild and Convenient Oxidation Procedure for the Conversion of Organoboranes to the Corresponding Alcohols. / Kabalka, George; Hedgecock, Herbert C.

In: Journal of Organic Chemistry, Vol. 40, No. 12, 01.06.1975, p. 1776-1779.

Research output: Contribution to journalArticle

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