HIGHLY STEREOSELECTIVE SYNTHESIS OF DIALKYL 2-ALKYLIDENE GLUTARATES
摘要:
Nucleophelic substitution of dialkyl (E)-2-bromomethylene glutarates 2 by magnesium dialkyl cuprates generated in situ provided a regio and highly stereoselective methodology for the synthesis of dialkyl 3-alkylidene glutarates 3 in good yields.
HIGHLY STEREOSELECTIVE SYNTHESIS OF DIALKYL 2-ALKYLIDENE GLUTARATES
作者:Ali Samarat、Jacques Lebreton、Hassen Amri
DOI:10.1081/scc-100103986
日期:2001.1
Nucleophelic substitution of dialkyl (E)-2-bromomethylene glutarates 2 by magnesium dialkyl cuprates generated in situ provided a regio and highly stereoselective methodology for the synthesis of dialkyl 3-alkylidene glutarates 3 in good yields.