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Deprotection Reagents in Fmoc Solid Phase Peptide Synthesis: Moving Away from Piperidine?
The deprotection step is crucial in order to secure a good quality product in Fmoc solid phase peptide synthesis. 9-Fluorenylmethoxycarbonyl (Fmoc) removal is achieved by a two-step mechanism reaction favored by the use of cyclic secondary amines; however, the efficiency of the reaction could be aff...
Autores principales: | Luna, Omar F., Gomez, Johana, Cárdenas, Constanza, Albericio, Fernando, Marshall, Sergio H., Guzmán, Fanny |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274427/ https://www.ncbi.nlm.nih.gov/pubmed/27854291 http://dx.doi.org/10.3390/molecules21111542 |
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