Chakraborty, Tushar Kanti ; Sudhakar, Gangarajula (2006) Total synthesis of (+)-conagenin Tetrahedron Letters, 47 (33). pp. 5847-5849. ISSN 0040-4039
Full text not available from this repository.
Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2006.06.087
Abstract
The total synthesis of the immunomodulator, (+)-conagenin was achieved using, as a key step, a method developed by us for the synthesis of 2-methyl-1,3-diols via Ti(III)-mediated diastereo- and regioselective opening of trisubstituted 2,3-epoxy alcohols, to carry out the stereoselective construction of its pentanoic acid segment.
Item Type: | Article |
---|---|
Source: | Copyright of this article belongs to Elsevier Science. |
Keywords: | Conagenin; Epoxide Opening; 2-Methyl-1; 3-diol; Immunomodulator |
ID Code: | 20505 |
Deposited On: | 20 Nov 2010 14:24 |
Last Modified: | 20 Nov 2010 14:24 |
Repository Staff Only: item control page