| Literature DB >> 17107057 |
Monica Vargas-Sanchez1, Sami Lakhdar, François Couty, Gwilherm Evano.
Abstract
The reaction of an azetidine with a chloroformate can give either the dealkylated heterocycle or the ring-opened product (gamma-chloroamine), which can further cyclize to the oxazinanone. A general study of this underrated reaction was conducted and revealed that azetidines can undergo smooth nucleophilic ring-opening reactions to highly functionalized gamma-chloroamines in the presence of a variety of alkyl chloroformates under mild reaction conditions. Yields are usually good, and parameters governing this reaction were evaluated. [reaction: see text].Entities:
Year: 2006 PMID: 17107057 DOI: 10.1021/ol062128c
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005