SQUALESTATIN SYNTHETIC STUDIES - TETHERED CONTROL IN A BICYCLOKETALISATION STEP

Authors
REID AM STEEL PG
Citation
Am. Reid et Pg. Steel, SQUALESTATIN SYNTHETIC STUDIES - TETHERED CONTROL IN A BICYCLOKETALISATION STEP, Journal of the Chemical Society. Perkin transactions. I (Print), (17), 1998, pp. 2795-2801
Citations number
26
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I (Print) → ACNP
ISSN journal
0300922X
Issue
17
Year of publication
1998
Pages
2795 - 2801
Database
ISI
SICI code
0300-922X(1998):17<2795:SSS-TC>2.0.ZU;2-Q
Abstract
A synthesis of an analogue of the dioxabicyclo[3.2.1]octane core struc ture of the squalestatins is reported in which control of the bicyclok etalisation is achieved by a tethering strategy.