| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269335 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
The marine β-carboline alkaloid eudistomin X has been synthesised stereospecifically, using d-phenylalanine as the chiral pool starting material, establishing the absolute configuration of the natural product as (10R).
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Rhys Finlayson, Amira Brackovic, Annabel Simon-Levert, Bernard Banaigs, Ronan F. O'Toole, Christopher H. Miller, Brent R. Copp,