Chemicals

(+)-Diethyl L-tartrate is used as a chiral auxiliary in the Sharpless enantioselective epoxidation of allylic alcohols, for Sharpless-type enantioselective oxidation of sulfides to sulfoxides and as a chiral auxiliary in the enantioselective

(+)-Diethyl L-tartrate is used as a chiral auxiliary in the Sharpless enantioselective epoxidation of allylic alcohols, for Sharpless-type enantioselective oxidation of sulfides to sulfoxides and as a chiral auxiliary in the enantioselective

(+)-Diethyl L-tartrate is used as a chiral auxiliary in the Sharpless enantioselective epoxidation of allylic alcohols, for Sharpless-type enantioselective oxidation of sulfides to sulfoxides and as a chiral auxiliary in the enantioselective

(+)-Dihydrocarvone (mixture of isomers) is a monoterpenoid compound, mainly used as a building block to prepare sesquiterpenes.

(+)-Dihydrocarvone (mixture of isomers) is a monoterpenoid compound, mainly used as a building block to prepare sesquiterpenes.

(+)-Dihydrocarvone (mixture of isomers) is a monoterpenoid compound, mainly used as a building block to prepare sesquiterpenes.

(+)-Dihydrocarvone (mixture of isomers) is a monoterpenoid compound, mainly used as a building block to prepare sesquiterpenes.

Description(+)-Dihydrocarvone, a monoterpenoid compound found in caraway oil, is a key building block to synthesize sesquiterpenes. It is generally produced either by the hydrogenation of carvone or oxidation of limonene.(+)-Dihydrocarvone may be

Description(+)-Dihydrocarvone, a monoterpenoid compound found in caraway oil, is a key building block to synthesize sesquiterpenes. It is generally produced either by the hydrogenation of carvone or oxidation of limonene.(+)-Dihydrocarvone may be

Description(+)-Dihydrocarvone, a monoterpenoid compound found in caraway oil, is a key building block to synthesize sesquiterpenes. It is generally produced either by the hydrogenation of carvone or oxidation of limonene.(+)-Dihydrocarvone may be

Both D- and L-forms are reagents for kinetic resolution of racemic allylic alcohols and α-furfuryl amides by enantioselective epoxidation.

Both D- and L-forms are reagents for kinetic resolution of racemic allylic alcohols and α-furfuryl amides by enantioselective epoxidation.