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Issue 19, 2000
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Enantiospecific total synthesis of both enantiomers of 2-thiocyanatoneopupukeanane from (R )-carvone

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Abstract

Enantiospecific synthesis of both enantiomers of the marine sesquiterpene 2-thiocyanatoneopupukeanane starting from (R)-carvone, employing an intramolecular rhodium carbenoid C–H insertion reaction as the key step, is described.

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Article information


Submitted
24 Jul 2000
Accepted
18 Aug 2000
First published
06 Sep 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 3191-3193
Article type
Communication

Enantiospecific total synthesis of both enantiomers of 2-thiocyanatoneopupukeanane from (R )-carvone

A. Srikrishna and S. J. Gharpure, J. Chem. Soc., Perkin Trans. 1, 2000, 3191
DOI: 10.1039/B005943I

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