Welcome to LookChem.com Sign In|Join Free

Article Doi

Enantioselective synthesis of cadinanes starting from R-(-)- or S-(+)- carvone

DOI: 10.1016/S0040-4020(98)00234-8

Source and publish data:

Tetrahedron p. 5623 - 5634 (1998)

Update date:2022-08-03

Topics:

Authors:

Baranovsky, Alexander V.Baranovsky, Alexander V.

Jansen, Ben J. M.Jansen, Ben J. M.

Meulemans, Tommi M.Meulemans, Tommi M.

De Groot, AedeDe Groot, Aede

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4020(98)00234-8

A new enantioselective synthesis of cadinanes, using the Mukaiyama- Michael reaction, was developed starting from R-(-)- or S-(+)-carvone. This approach gives an easy and direct access to the cadinane skeleton and the scope proved to be complementary to a

View More

Full text of DOI:10.1016/S0040-4020(98)00234-8

Products guided by the article

Product name:(2S,2'R,3R)-3-isopropenyl-6-methyl-2-(2'-methyl-3'-oxo-butyl)-5-cyclohexen-1-one

Cas No:207922-78-9

207922-78-9

R&D Labs maybe for 207922-78-9

Relevant to this article

Hot Product