Publication details

Stereoselective synthesis of alpha-alkylidene- and substituted alkylidene-gamma-lactones

Authors

ČASTULÍK Jakub MAZAL Ctibor

Year of publication 2000
Type Article in Periodical
Magazine / Source Tetrahedron Letters
MU Faculty or unit

Faculty of Science

Citation
Web http://www.elsevier.nl/inca/publications/store/2/3/3/
Field Organic chemistry
Keywords methylene lactones; coupling reactions; palladium; zinc compounds
Description Cross-coupling reactions of (E)- and (Z)-tosylates of alpha-hydroxymethylene-gamma-butyrolactone with aryl, heteroaryl, alkyl, and alkynylzinc chlorides under Pd(PPh3)4 catalysis were found to be a suitable synthetic method for stereoselective preparation of alpha-alkylidene- and substituted alkylidene-gamma-lactones. Reactions, conducted under mild conditions, proceed with high stereoselectivity and moderate yields.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info