| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5226963 | Tetrahedron | 2007 | 5 Pages |
Abstract
The first total synthesis of the rearranged aromatic sesquiterpene (±)-laurokamurene B, isolated from the Chinese red alga Laurencia okamurai Yamada, has been accomplished, confirming the structure of the natural product. A combination of Ireland-Claisen rearrangement and ring-closing metathesis was employed as key reactions.
Graphical abstract
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
A. Srikrishna, I.A. Khan, R. Ramesh Babu, A. Sajjanshetty,