Stereoselective synthesis of (+)-isoindolo-beta-carboline

TitleStereoselective synthesis of (+)-isoindolo-beta-carboline
Publication TypeJournal Article
Year of Publication2009
AuthorsWakchaure, PB, Puranik, VG, Argade, NP
JournalTetrahedron-Asymmetry
Volume20
Issue2
Pagination220-224
Date PublishedFEB
ISSN0957-4166
Abstract

Starting from homophthalic anhydride and (S)-tryptophan, the stereoselective synthesis of (+)-isoindolo-beta-carboline has been described via the corresponding homophthalimide, its chemoselective oxidative ring contraction, and the intramolecular dehydrative ring closure followed by a geometry-specific demethoxycarbonylation. (C) 2009 Elsevier Ltd. All rights reserved.

DOI10.1016/j.tetasy.2009.01.001
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)2.484
Divison category: 
Center for Material Characterization (CMC)
Organic Chemistry