Synthesis of 3-Thia-1-dethiacephems via Regioselective Iodocyclization Reaction

TitleSynthesis of 3-Thia-1-dethiacephems via Regioselective Iodocyclization Reaction
Publication TypeJournal Article
Year of Publication2015
AuthorsGarud, DR, Rode, ND, Bathe, SR, Ranpise, VS, Joshi, RA, Joshi, RR, Koketsu, M
JournalSynthesis-Stuttgart
Volume47
Issue24
Pagination3956-3962
Date PublishedDEC
ISSN0039-7881
Keywords-lactams, 3-thia-1-dethiacephems, Iodocyclization, Regioselective, thiourea
Abstract

The key N-homopropargylthiourea intermediates, N-substituted 2-oxo-4-propargylazetidine-1-carbothioamides, were prepared by the reaction of a 4-propargylazetidin-2-one with isothiocyanates. Bicyclic -lactams, i.e. 3-thia-1-dethiacephems, were prepared via highly regioselective iodocyclization reaction of N-substituted 2-oxo-4-propargylazetidine-1-carbothioamides with molecular iodine at room temperature in moderate to excellent yields. A variety of functional groups were well tolerated under the reaction conditions.

DOI10.1055/s-0035-1560350
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)2.652
Divison category: 
Organic Chemistry