Tetrahedron p. 5623 - 5634 (1998)
Update date:2022-08-03
Topics:
Baranovsky, Alexander V.
Jansen, Ben J. M.
Meulemans, Tommi M.
De Groot, Aede
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
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Doi:10.1007/BF01185910
(1965)Doi:10.1002/cjoc.201300924
(2014)Doi:10.1002/anie.201505740
(2015)Doi:10.1055/s-1998-1761
(1998)Doi:10.1021/jo0355350
(2004)Doi:10.1021/ja01023a024
(1968)
