DIELS-ALDER REACTIONS OF METHYL N-P-METHOXYBENZENSULFONYLINDOLE-2-(2-PROPENOATE), A CONVENIENT DIENOPHILE TOWARDS THE SYNTHESIS OF ANDRANGININE

Authors
DANIELI B LESMA G LUZZANI M PASSARELLA D SILVANI A
Citation
B. Danieli et al., DIELS-ALDER REACTIONS OF METHYL N-P-METHOXYBENZENSULFONYLINDOLE-2-(2-PROPENOATE), A CONVENIENT DIENOPHILE TOWARDS THE SYNTHESIS OF ANDRANGININE, Tetrahedron, 52(34), 1996, pp. 11291-11296
Citations number
16
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
52
Issue
34
Year of publication
1996
Pages
11291 - 11296
Database
ISI
SICI code
0040-4020(1996)52:34<11291:DROMN>2.0.ZU;2-Y
Abstract
Methyl N-p-methoxybenzensulfonylindole-2-(2-propenoate) (2) undergoes Diels-Alder reactions with silyloxybutadienes and 5-ethenylpyridinones to afford advanced intermediates for the total synthesis of (+/-)-and ranginine (1). Copyright (C) 1996 Published by Elsevier Science Ltd