Chakraborty, Tushar K. ; Tapadar, Subhasish (2001) Diastereoselective opening of trisubstituted epoxy alcohols: application in the synthesis of (+)-prelactone C Tetrahedron Letters, 42 (7). pp. 1375-1377. ISSN 0040-4039
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...
Related URL: http://dx.doi.org/10.1016/S0040-4039(00)02247-4
Abstract
A novel method developed by us for the synthesis of chiral 2-methyl-1,3-diols by radical-mediated diastereoselective opening of trisubstituted epoxy alcohols at the more substituted carbon was the key step in the synthesis of (+)-prelactone C (1).
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 20609 |
| Deposited On: | 20 Nov 2010 13:53 |
| Last Modified: | 22 May 2011 15:50 |
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