BAEYER-VILLIGER OXIDATION OF NORBORNAN-7-ONES - LONG-RANGE SUBSTITUENT EFFECTS ON REGIOSELECTIVITY

Authors
MEHTA G MOHAL N
Citation
G. Mehta et N. Mohal, BAEYER-VILLIGER OXIDATION OF NORBORNAN-7-ONES - LONG-RANGE SUBSTITUENT EFFECTS ON REGIOSELECTIVITY, Journal of the Chemical Society. Perkin transactions. I, (3), 1998, pp. 505-507
Citations number
12
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I → ACNP
ISSN journal
0300922X
Issue
3
Year of publication
1998
Pages
505 - 507
Database
ISI
SICI code
0300-922X(1998):3<505:BOON-L>2.0.ZU;2-9
Abstract
The regioselectivity of the Baeyer-Villiger oxidation of norbornan-7-o nes can be steered by the distal 2-endo-substituents present. Hydrolys is of the resulting bicyclic lactones provides a stereospecific route to functionalized cyclohexanes.