SULFUR EXTRUSION REACTION - A VERSATILE CYCLIC BETA-ENAMINO ESTER SYNTHESIS FROM SECONDARY ALPHA-BROMO ESTERS

Authors
MARCHAND P FARGEAUBELLASSOUED MC BELLEC C LHOMMET G
Citation
P. Marchand et al., SULFUR EXTRUSION REACTION - A VERSATILE CYCLIC BETA-ENAMINO ESTER SYNTHESIS FROM SECONDARY ALPHA-BROMO ESTERS, Synthesis, (11), 1994, pp. 1118-1120
Citations number
15
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthesis → ACNP
ISSN journal
00397881
Issue
11
Year of publication
1994
Pages
1118 - 1120
Database
ISI
SICI code
0039-7881(1994):11<1118:SER-AV>2.0.ZU;2-A
Abstract
Various commercial secondary alpha-bromo esters 2 react with five-memb ered thiolactams 1 in a direct sulfur extrusion reaction to give N-alk ylated tetrasubstituted cyclic beta-enamino esters 4 in good yields.