DIASTEREOSELECTIVE ANOMERIC OXYGEN TO CARBON REARRANGEMENTS OF SILYL ENOL ETHER DERIVATIVES OF LACTOLS

Authors
DIXON DJ LEY SV TATE EW
Citation
Dj. Dixon et al., DIASTEREOSELECTIVE ANOMERIC OXYGEN TO CARBON REARRANGEMENTS OF SILYL ENOL ETHER DERIVATIVES OF LACTOLS, Synlett, (10), 1998, pp. 1093
Citations number
7
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
10
Year of publication
1998
Database
ISI
SICI code
0936-5214(1998):10<1093:DAOTCR>2.0.ZU;2-J
Abstract
Lewis acid promoted oxygen to carbon rearrangement of anomerically lin ked silyl enol ethers gives a new and diastereoselective route to the corresponding 2-alpha-hydroxyketone substituted products.