Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5266570 | Tetrahedron Letters | 2011 | 5 Pages |
Abstract
A new strategy for the synthesis of 1,2-dideoxy iminosugar C-glycosides and indolizidines involving highly stereoselective [2,3]-Wittig rearrangement from Garner aldehyde has been developed. This rearrangement yielded an optically pure, highly functionalized key intermediate, which has been further utilized for the synthesis of 5-epi-ethylfagomine, 2-epi-5-deoxyadenophorine, and 5-hydroxymethyl indolizidine.
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Authors
B. Chandrasekhar, J. Prasada Rao, B. Venkateswara Rao, P. Naresh,