Sabitha, Gowravaram ; Gopal, Peddabuddi ; Nagendra Reddy, C. ; Yadav, Jhillu S. (2009) A concise and efficient synthesis of (5R,7S)-kurzilactone and its (5S,7R)-enantiomer by the Mukaiyama aldol reaction Synthesis, 19 . pp. 3301-3304. ISSN 0039-7881
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Official URL: https://www.thieme-connect.com/ejournals/abstract/...
Related URL: http://dx.doi.org/10.1055/s-0029-1216936
Abstract
Natural kurzilactone (5R,7S) and its (5S,7R)-enantiomer were synthesized by a convergent approach using a diastereoselective Mukaiyama aldol reaction to construct the anti diol unit. Finally, a ring-closing metathesis reaction led to the target molecule.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Thieme Medical Publishers. |
| Keywords: | Kurzilactone; Mukaiyama Reaction; Aldol Reaction; Ring Closure; Metathesis |
| ID Code: | 63174 |
| Deposited On: | 28 Sep 2011 03:39 |
| Last Modified: | 28 Sep 2011 03:39 |
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