Total synthesis of umuravumbolide and hyptolide through silicon-tethered ring-closing metathesis
Title | Total synthesis of umuravumbolide and hyptolide through silicon-tethered ring-closing metathesis |
Publication Type | Journal Article |
Year of Publication | 2013 |
Authors | Chowdhury, PSarathi, Kumar, P |
Journal | European Journal of Organic Chemistry |
Volume | 2013 |
Issue | 21 |
Pagination | 4586-4593 |
Date Published | JUL |
ISSN | 1434-193X |
Keywords | lactones, Metathesis, Silanes, synthetic methods, Total synthesis, Wittig reactions |
Abstract | The total synthesis of umuravumbolide and hyptolide has been achieved in a efficient manner by using temporary silicon-tethered ring-closing metathesis and cross-coupling reactions as key steps. The stereogenic centres were generated by means of proline-catalysed -aminoxylation of aldehydes and Brown's asymmetric allylation method. |
DOI | 10.1002/ejoc.201300302 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 3.154 |
Divison category:
Organic Chemistry