Abstract
The application of dithiocarbamates in group transfer radical cyclization reactions is described. Carbamoyl diethyldithiocarbamates are synthesized in two high-yielding steps from secondary amines and act as sources of carbamoyl radicals through chemical or photochemical initiation. Group transfer radical cyclization reactions lead to dithiocarbamate-functionalized lactams. (c) 2007 Wiley Periodicals, Inc.
Original language | English |
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Pages (from-to) | 568-571 |
Number of pages | 1 |
Journal | Heteroatom Chemistry |
Volume | 18 |
Issue number | 5 |
DOIs | |
Publication status | Published - 10 Jul 2007 |