Preparation of ethyl 6-methoxy-7-methyl-1-aryl/cyclohexyl-4-oxo-2-naphthoates as an intermediates for synthesis of beta-apopicropodophyllin analogues

Citation
N. Nanjundaswamy et al., Preparation of ethyl 6-methoxy-7-methyl-1-aryl/cyclohexyl-4-oxo-2-naphthoates as an intermediates for synthesis of beta-apopicropodophyllin analogues, I J CHEM B, 40(4), 2001, pp. 274-277
Citations number
10
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY
ISSN journal
03764699 → ACNP
Volume
40
Issue
4
Year of publication
2001
Pages
274 - 277
Database
ISI
SICI code
0376-4699(200104)40:4<274:POE6>2.0.ZU;2-A
Abstract
Preparation of tetralone ester 4a-c, an intermediate for the synthesis of b eta -apopicropodophyllin analogues via Stobbe condensation of benzophenone derivatives followed by Friedel Craft's cyclization is described.