Abstract
Synthesis of the C3-C10 and C13-C21 segments, having seven asymmetric centers of the marine macrolide, (-)-laulimalide is reported. The requisite stereogenic centers were generated on the chirons by the application of asymmetric reactions.
Keywords: intramolecular cyclization, chiron, stereoselective synthesis, Sharpless asymmetric epoxidation, laulimalide, Marine macrolide
Letters in Organic Chemistry
Title: Stereoselective Synthesis of C3-C10 and C13-C21 Fragments of Laulimalide
Volume: 3 Issue: 6
Author(s): Ajit Chand Kunwar, Gangavaram V. M. Sharma, Anabathula Prabhakar and Sreenivas Punna
Affiliation:
Keywords: intramolecular cyclization, chiron, stereoselective synthesis, Sharpless asymmetric epoxidation, laulimalide, Marine macrolide
Abstract: Synthesis of the C3-C10 and C13-C21 segments, having seven asymmetric centers of the marine macrolide, (-)-laulimalide is reported. The requisite stereogenic centers were generated on the chirons by the application of asymmetric reactions.
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Cite this article as:
Chand Kunwar Ajit, M. Sharma V. Gangavaram, Prabhakar Anabathula and Punna Sreenivas, Stereoselective Synthesis of C3-C10 and C13-C21 Fragments of Laulimalide, Letters in Organic Chemistry 2006; 3 (6) . https://dx.doi.org/10.2174/157017806777828411
DOI https://dx.doi.org/10.2174/157017806777828411 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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