NOVEL CHEMISTRY OF THE IMDA ADDUCTS OF THE AMIDES DERIVED FROM DICHLOROMALEIC ANHYDRIDE AND BETA-AMINOMETHYLSTYRENES

Citation
Jr. Dawson et Jm. Mellor, NOVEL CHEMISTRY OF THE IMDA ADDUCTS OF THE AMIDES DERIVED FROM DICHLOROMALEIC ANHYDRIDE AND BETA-AMINOMETHYLSTYRENES, Tetrahedron letters, 36(49), 1995, pp. 9043-9046
Citations number
24
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
36
Issue
49
Year of publication
1995
Pages
9043 - 9046
Database
ISI
SICI code
0040-4039(1995)36:49<9043:NCOTIA>2.0.ZU;2-4
Abstract
Reaction of amides derived from dichloromaleic anhydride and beta-amin omethylstyrenes affords unstable Diels Alder adducts, which give via c ompeting processes a number of products including pyrrolidinones by a novel sequence of dehydrochlorination and subsequent ring-opening of a cyclohexadiene.