Dithiocarbamate group transfer cyclization reactions of carbomoyl radicals under "tin-free" conditions

Richard Grainger, P Innocenti

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

Oxygen or nitrogen? Radical chemists overwhelmingly choose to work with xanthates rather than dithiocarbamates, yet the latter offer a distinct advantage in the case of a new method for generating carbamoyl radicals. Functionalized lactams of various ring sizes can be prepared in an operationally simple procedure involving irradiation or heating in the presence of a radical initiator (see scheme).
Original languageEnglish
Pages (from-to)3445-3448
Number of pages4
JournalAngewandte Chemie (International Edition)
Volume43
DOIs
Publication statusPublished - 22 Jun 2004

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