81669-02-5Relevant articles and documents
REACTION OF LITHIUM DIMETHYLCUPRATE WITH CONFORMATIONALLY BIASED β-ACYLOXY ENOL ESTERS - REGIO AND STEREOCONTROLLED ACCESS TO FUNCTIONALIZED SIX-CARBON CHIRAL SYNTHONS
Hanessian, Stephen,Tyler, Peter C.,Chapleur, Yves
, p. 4583 - 4586 (2007/10/02)
Alkyl 2-acyloxy α-D-erythro-hex-2-enopyranoside diesters, readily available from D-hexoses, are versatile intermediates for the expeditious preparation of six-carbon chiral synthons containing alternating and/or consecutive C-methyl and hydroxyl groups.