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...
Abstract
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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