| Literature DB >> 15200320 |
Michael Harmata1, Xuechuan Hong, Charles L Barnes.
Abstract
[reaction: see text] The tricyclic benzothiazine 15 was prepared in a straightforward fashion via a completely stereoselective intramolecular Friedel-Crafts alkylation. This compound represents a potential precursor to the antitubercular agent, pseudopteroxazole. Its synthesis proceeded via a completely selective, intramolecular addition of a sulfoximine-stabilized carbanion to an alpha,beta-unsaturated ester, followed by functional group manipulations.Entities:
Year: 2004 PMID: 15200320 DOI: 10.1021/ol049334+
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005