Intramolecular chemoselective acylation of a suitably substituted isoindole: synthesis of (+/-)-chilenine and (+/-)-deoxychilenine

TitleIntramolecular chemoselective acylation of a suitably substituted isoindole: synthesis of (+/-)-chilenine and (+/-)-deoxychilenine
Publication TypeJournal Article
Year of Publication2011
AuthorsWakchaure, PB, Argade, NP
JournalSynthesis-Stuttgart
Issue17
Pagination2838-2842
Date PublishedSEP
ISSN0039-7881
Keywordschemoselective acylation, chilenine, deoxychilenine, homophthalic anhydride, isoindole, Total synthesis
Abstract

Starting from 3,4-dimethoxyhomophthalic anhydride and 6-bromohomopiperonylamine, concise and efficient syntheses of Chilean berberis products chilenine and deoxychilenine have been demonstrated via partially divergent routes by taking advantage of facile air-oxidation of homophthalimide along with intramolecular chemoselective acylation as the key steps.

DOI10.1055/s-0030-1260140
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)2.466
Divison category: 
Organic Chemistry