| Literature DB >> 12713316 |
Amy S Ripka1, David D Díaz, K Barry Sharpless, M G Finn.
Abstract
Isonitriles and ureas undergo a condensation reaction in the presence of acid chlorides to give formamidine ureas, for which no general synthetic routes currently exist. A mechanism is proposed in which the key intermediate is an electrophilic adduct of isonitrile and acid chloride. The process is tolerant of moderate variability in the nature of the components, and access to formamidine ureas of varying substitution patterns is further enhanced by a facile exchange reaction with amines. [reaction: see text]Entities:
Mesh:
Substances:
Year: 2003 PMID: 12713316 DOI: 10.1021/ol034287r
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005