Chandrasekhar, S. ; Ramachandar, T. ; Venkateswara Rao, B. (2001) Chiron approach to callipeltin A: first synthesis of fully protected (2R,3R,4S)-4,7-diamino-2,3-dihydroxy heptanoic acid Tetrahedron: Asymmetry, 12 (16). pp. 2315-2321. ISSN 0957-4166
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/S0957-4166(01)00400-1
Abstract
Stereoselective synthesis of protected (2R,3R,4S)-4,7-diamino-2,3-dihydroxy heptanoic acid, which is present as a side chain attached to the main macrocyclic depsidecapeptide backbone of callipeltin A (a potent, cytotoxic, anti-HIV and anti-fungal agent) starting from a carbohydrate, is described.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 63496 |
| Deposited On: | 29 Sep 2011 04:16 |
| Last Modified: | 29 Sep 2011 04:16 |
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