NOVEL TRI-N-BUTYLTIN HYDRIDE-AZOISOBUTYRONITRILE-INDUCED INTRAMOLECULAR RING-CLOSURE REACTION - A CONVENIENT SYNTHESIS OF SUBSTITUTED AZETIDIN-3-ONES

Authors
CHOWDHURY AR KUMAR VV ROY R BHADURI AP
Citation
Ar. Chowdhury et al., NOVEL TRI-N-BUTYLTIN HYDRIDE-AZOISOBUTYRONITRILE-INDUCED INTRAMOLECULAR RING-CLOSURE REACTION - A CONVENIENT SYNTHESIS OF SUBSTITUTED AZETIDIN-3-ONES, Journal of chemical research. Synopses, (7), 1997, pp. 254-255
Citations number
11
Categorie Soggetti
Chemistry
Journal title
Journal of chemical research. Synopses → ACNP
ISSN journal
03082342
Issue
7
Year of publication
1997
Pages
254 - 255
Database
ISI
SICI code
0308-2342(1997):7<254:NTHI>2.0.ZU;2-1
Abstract
Tri-n-butyltin hydride-azoisobutyronitrile-mediated intramolecular rin g-closure reactions yield 2-cyano-1,2-di(phenyl or substituted phenyl) azetidin-3-ones; N-15 NMR studies support the assigned structures.