Stereoselective synthesis of the densely functionalized C1-C9 fragment of amphidinolides C and F
Title | Stereoselective synthesis of the densely functionalized C1-C9 fragment of amphidinolides C and F |
Publication Type | Journal Article |
Year of Publication | 2009 |
Authors | Mohapatra, DK, Dasari, P, Rahaman, H, Pal, R |
Journal | Tetrahedron Letters |
Volume | 50 |
Issue | 46 |
Pagination | 6276-6279 |
Date Published | NOV |
ISSN | 0040-4039 |
Keywords | Amphidinolide C and F, Cytotoxic, Tandem dihydroxylation-S(N)2, Wacker oxidation, Wittig reaction |
Abstract | The synthesis of the C1-C9 subunit of amphidinolides C and F is described. Key steps include tandem Sharpless asymmetric dihydroxylation-S(N)2 cyclization reaction, Lewis acid-mediated epoxide opening, Wittig reaction, and Wacker oxidation. (C) 2009 Elsevier Ltd. All rights reserved. |
DOI | 10.1016/j.tetlet.2009.09.001 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 2.618 |
Divison category:
Organic Chemistry