A STRAIGHTFORWARD AND PRACTICAL FORMAL SYNTHESIS OF LAVENDAMYCIN ETHYL-ESTER

Authors
MOLINA P MURCIA F FRESNEDA PM
Citation
P. Molina et al., A STRAIGHTFORWARD AND PRACTICAL FORMAL SYNTHESIS OF LAVENDAMYCIN ETHYL-ESTER, Tetrahedron letters, 35(9), 1994, pp. 1453-1456
Citations number
24
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
9
Year of publication
1994
Pages
1453 - 1456
Database
ISI
SICI code
0040-4039(1994)35:9<1453:ASAPFS>2.0.ZU;2-X
Abstract
Aza Wittig reaction of iminophosphorane derived from ethyl alpha-azido -beta-(3-indolyl)butyrate and 8-benzyloxy-7-bromo-2-formylquinoline is the key step in a new synthesis of lavendamycin ethyl ester.