| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5264187 | Tetrahedron Letters | 2013 | 6 Pages |
Abstract
The first stereoselective total synthesis of the marine-derived antimicrobial amino-alcohols, crucigasterins A, B and D has been accomplished through a common intermediate starting from pent-3-en-1-ol. The method involves the Sharpless asymmetric aminohydroxylation and Julia and Wittig olefinations as the key steps.
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Authors
Jayprakash Narayan Kumar, Biswanath Das,