Yadav, J. S. ; Raju, A. ; Ravindar, K. ; Subba Reddy, B. V. (2010) Stereoseletive total synthesis of 11-α-and 11-β-methoxycurvularins Synthesis, 2010 (5). pp. 797-802. ISSN 0039-7881
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Official URL: http://www.thieme-connect.com/ejournals/abstract/s...
Related URL: http://dx.doi.org/10.1055/s-0029-1218621
Abstract
Total synthesis of 11-α-methoxycurvularin and 11-β-methoxycurvularin has been accomplished in a highly stereoselective manner by utilizing Jacobsen hydrolytic kinetic resolution, Maruoka asymmetric allylation and intramolecular Friedel-Crafts acylation as key steps.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Thieme Medical Publishers. |
| Keywords: | 11-α-methoxycurvularin; 11-β-methoxycurvularin; Jacobsen Resolution; Maruoka Asymmetric Allylation; Intramolecular Friedel-Crafts Acylation |
| ID Code: | 63117 |
| Deposited On: | 28 Sep 2011 03:45 |
| Last Modified: | 28 Sep 2011 03:45 |
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