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Facile Enantiospecific Synthesis of Dihydroconduritols E and F

Prasad, Kavirayan R and Pawar, Amit B (2008) Facile Enantiospecific Synthesis of Dihydroconduritols E and F. In: Synthesis- Stutgart (19). pp. 3155-3159.

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Official URL: http://www.thieme-connect.de/DOI/DOI?10.1055/s-200...


An enantiospecific synthesis of cyclohexane-1,2,3,4-tetrols was accomplished from l-(+)-tartaric acid. Pivotal steps in the synthetic sequence include zinc-mediated Boord-type fragmentation of an acetonide, ring-closing metathesis (RCM), and osmium-mediated dihydroxylation.

Item Type: Journal Article
Publication: Synthesis- Stutgart
Publisher: Thieme Medical Publishers
Additional Information: Copyright of this article belongs to Thieme Medical Publishers.
Keywords: Natural-Products ;Cyclitolls;Methathesis;Acid.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 19 Jul 2009 08:20
Last Modified: 19 Jul 2009 08:20
URI: http://eprints.iisc.ac.in/id/eprint/16478

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