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An efficient route for the synthesis of methyl (-)-1,4a-dimethyl-5-oxodecahydronaphthalene-1-carboxylate by using baker's yeast-catalyzed asymmetric reduction

Journal

TETRAHEDRON-ASYMMETRY
Volume 17, Issue 11, Pages 1655-1662

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2006.06.015

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Methyl (-)-1,4a-dimethyl-5-oxodecahydronaphthalene-1-carboxylate 1, a key synthetic intermediate for the synthesis of terpenoids, was efficiently synthesized by using a baker's yeast-catalyzed asymmetric reduction of a sigma-symmetrical 1,3-cyclohexanedione derivative. (c) 2006 Elsevier Ltd. All rights reserved.

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