A Mild and Convenient Procedure for Conversion of Alkenes into Alkyl Iodides via Reaction of Iodine Monochloride with Organoboranes

George Kabalka, E. Eugene Gooch

Research output: Contribution to journalArticle

58 Citations (Scopus)

Abstract

Alkenes are rapidly converted to alkyl iodides under mild conditions via a hydroboration-iodination sequence which utilizes iodine monochloride as the iodinating agent. The iodination proceeds with inversion of configuration. A series of functionally substituted iodides was synthesized via the new procedure.

Original languageEnglish (US)
Pages (from-to)3578-3580
Number of pages3
JournalJournal of Organic Chemistry
Volume45
Issue number18
DOIs
StatePublished - Jan 1 1980
Externally publishedYes

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Alkenes
Iodides
iodine monochloride

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

A Mild and Convenient Procedure for Conversion of Alkenes into Alkyl Iodides via Reaction of Iodine Monochloride with Organoboranes. / Kabalka, George; Gooch, E. Eugene.

In: Journal of Organic Chemistry, Vol. 45, No. 18, 01.01.1980, p. 3578-3580.

Research output: Contribution to journalArticle

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