Trimethylsilyl Esters

Protection of Carboxylic Acids during Hydroboration Reactions

George Kabalka, Donald E. Bierer

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Trimethylsilyl esters of carboxylic acids are inert to a variety of hydroborating agents and provide a convenient method for protecting the acid functionality during organoborane transformations.

Original languageEnglish (US)
Pages (from-to)655-659
Number of pages5
JournalOrganometallics
Volume8
Issue number3
DOIs
StatePublished - Jan 1 1989
Externally publishedYes

Fingerprint

hydroboration
Carboxylic Acids
carboxylic acids
esters
Esters
acids
Acids

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

Cite this

Trimethylsilyl Esters : Protection of Carboxylic Acids during Hydroboration Reactions. / Kabalka, George; Bierer, Donald E.

In: Organometallics, Vol. 8, No. 3, 01.01.1989, p. 655-659.

Research output: Contribution to journalArticle

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