Prasad, Kavirayani R. ; Pawar, Amit B. (2008) Facile enantiospecific synthesis of dihydroconduritols E and F Synthesis, 2008 (19). pp. 3155-3159. ISSN 0039-7881
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Official URL: https://www.thieme-connect.de/DOI/DOI?10.1055/s-20...
Related URL: http://dx.doi.org/10.1055/s-2008-1067261
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: | Article |
|---|---|
| Source: | Copyright of this article belongs to Thieme Medical Publishers Inc. |
| Keywords: | Cyclitols; Ring-closing Metathesis; Tartaric Acid; Boord Fragmentation |
| ID Code: | 105806 |
| Deposited On: | 21 Dec 2017 12:05 |
| Last Modified: | 21 Dec 2017 12:05 |
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