An enantiospecific synthesis of a crinipellin

Srikrishna, A and Gowri, V (2012) An enantiospecific synthesis of a crinipellin. In: Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry, 51 (3). pp. 481-485.

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Abstract

An enantiospecific synthesis of a crinipellin has been accomplished, starting from the readily available (S)-campholenaldehyde employing two intramolecular rhodium carbenoid CH insertions and an intramolecular Michael addition reaction as key steps.

Item Type:	Journal Article
Publication:	Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry
Publisher:	National Institute of Science Communication and Information Resources
Additional Information:	Copyright of this article belongs to National Institute of Science Communication and Information Resources.
Keywords:	Crinipellins;tetraquinanes;enantiospecific synthesis; campholenaldehyde;intramolecular Michael addition
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	25 Apr 2012 08:30
Last Modified:	25 Apr 2012 08:30
URI:	http://eprints.iisc.ac.in/id/eprint/44346

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