Vijaya Anand, R. ; Baktharaman, S. ; Singh, Vinod K. (2002) Elaboration of a Baylis–Hillman adduct to (−)-acaterin and its diastereomer through ring closing metathesis Tetrahedron Letters, 43 (31). pp. 5393-5395. ISSN 0040-4039
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/S0040-4039(02)01069-9
Abstract
A short and efficient synthesis of acaterin, a biologically important natural product has been achieved by elaboration of a Baylis-Hillman adduct. The key step for the synthesis is a ring closing metathesis reaction using Grubbs’ catalyst.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 55342 |
| Deposited On: | 18 Aug 2011 08:37 |
| Last Modified: | 18 Aug 2011 08:37 |
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