Journal article
Toward the Enantioselective Total Synthesis of Lyngbyatoxin A: On the Stereocontrolled Introduction of the Quaternary Stereogenic Centre
In
Tetrahedron
—
2003, Volume 59, Issue 35, pp. 6937-6945
Abstract
This paper deals with an approach to the enantioselective total synthesis of Lyngbyatoxin A, with focus on the stereocontrolled introduction of the quaternary stereogenic centre. The key step in the synthesis involves an enantiospecific Lewis-acid mediated rearrangement of chiral vinyl epoxides carrying a 7-substituted indole moiety.
| Language: | English |
|---|---|
| Year: | 2003 |
| Pages: | 6937-6945 |
| ISSN: | 14645416 and 00404020 |
| Types: | Journal article |
| DOI: | 10.1016/S0040-4020(03)00822-6 |
| ORCIDs: | Tanner, David Ackland |
