A CONVENIENT ROUTE TO SPIROPYRROLIDINYL-OXINDOLE ALKALOIDS VIA C-3 SUBSTITUTED ENE-PYRROLIDINE CARBAMATE RADICAL CYCLIZATION

Authors
COSSY J CASES M PARDO DG
Citation
J. Cossy et al., A CONVENIENT ROUTE TO SPIROPYRROLIDINYL-OXINDOLE ALKALOIDS VIA C-3 SUBSTITUTED ENE-PYRROLIDINE CARBAMATE RADICAL CYCLIZATION, Tetrahedron letters, 39(16), 1998, pp. 2331-2332
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
39
Issue
16
Year of publication
1998
Pages
2331 - 2332
Database
ISI
SICI code
0040-4039(1998)39:16<2331:ACRTSA>2.0.ZU;2-R
Abstract
A short access to spiropyrrolidinyl-oxindole alkaloids via a substitut ed ene-pyrrolidine carbamate, synthesized from the commercially availa ble tert-butyl 1-pyrrolidine carboxylate, is described. (C) 1998 Elsev ier Science Ltd. All rights reserved.