Ítem
| Ministerio de Ciencia e Innovación (Espanya) | |
|
Rosés Subirós, Cristina
Camó Marin, Cristina Vogels, Kristy Planas i Grabuleda, Marta Feliu Soley, Lídia |
|
|
The first solid-phase strategy for the synthesis of cyclic depsipeptides containing a phenyl ester linkage in their structure is described. The key steps of the synthesis were the formation of the phenyl ester bond and the on-resin head-to-side-chain cyclization. The amino acid configuration significantly influenced the formation and the stability of the cyclic depsipeptides. The presence of a l-Tyr1 and a d-Tyr7 led to the most stable sequences This work was financed by Grant AGL2012-39880-C02-02 |
|
| http://hdl.handle.net/2072/299088 | |
| eng | |
| American Chemical Society (ACS) | |
| Tots els drets reservats | |
|
Pèptids -- Síntesi
Peptides -- Synthesis Depsipèptid Depsipeptide |
|
| Solid-Phase Synthesis of Cyclic Depsipeptides Containing a Tyrosine Phenyl Ester Bond | |
| info:eu-repo/semantics/article | |
| Recercat |
