Please use this identifier to cite or link to this item:
https://dspace.lboro.ac.uk/2134/13937
|
| Title: | Total synthesis of the marine-derived cyclic depsipeptide alternaramide |
| Authors: | Horton, Alexandra E.
May, Oliver S.
Elsegood, Mark R.J.
Kimber, Marc C. |
| Keywords: | Natural product
Depsipeptide
Peptide coupling
Macrolactonization
Macrolactamization |
| Issue Date: | 2011 |
| Publisher: | © Georg Thieme Verlag |
| Citation: | HORTON, A.E. ... et al, 2011. Total synthesis of the marine-derived cyclic depsipeptide alternaramide. Synlett, 22 (6), pp. 797 - 800 |
| Abstract: | The first synthesis of the marine fungus derived natural product alternaramide is described using solution phase coupling protocols and via a macrolactonization and macrolactamization route. The structure of alternaramide was confirmed and was supported by single crystal X-ray analysis which exhibited three similar molecules in the asymmetric unit, each with transannular hydrogen bonds. |
| Description: | This article was published in the journal, Synlett [© Georg Thieme Verlag]. The definitive version is available at: http://dx.doi.org/10.1055/s-0030-1259915 |
| Version: | Accepted for publication |
| DOI: | 10.1055/s-0030-1259915 |
| URI: | https://dspace.lboro.ac.uk/2134/13937 |
| Publisher Link: | http://dx.doi.org/10.1055/s-0030-1259915 |
| ISSN: | 0936-5214 |
| Appears in Collections: | Published Articles (Chemistry)
|
Files associated with this item:
|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
|
