Chakraborty, Tushar Kanti ; Sudhakar, Gangarajula (2005) Stereoselective synthesis of the various isomers of 3,4-dideoxy furanoid sugar amino acids with methyl substitution at the C6 position Tetrahedron Letters, 46 (25). pp. 4287-4290. ISSN 0040-4039
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2005.04.094
Abstract
Various isomers of C6-methyl-containing chiral 3,4-dideoxy furanoid sugar amino acids were synthesized following a common strategy, in which the C2 and C6 chiral centres were derived from the chiralities of the two starting materials, glyceraldehyde acetonide and N,N-dibenzylalaninal, respectively, and the C5 centre was fixed by standard diastereoselective transformations.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Sugar Amino Acids; Amino Acids; Peptidomimetics; Dipeptide Isosteres |
| ID Code: | 20536 |
| Deposited On: | 20 Nov 2010 14:21 |
| Last Modified: | 20 Nov 2010 14:21 |
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