New TFA-Free Cleavage and Final Deprotection in Fmoc Solid-Phase Peptide Synthesis: Dilute HCl in Fluoro Alcohol
Author:
Affiliation:
1. Department of Chemistry, University of Reading, P.O. Box 224, Whiteknights, Reading RG6 6AD, U.K.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol303124r
Reference61 articles.
1. Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide
2. SOLID-PHASE PEPTIDE SYNTHESIS USING MILD BASE CLEAVAGE OF NαFLUORENYLMETHYLOXYCARBONYLAMINO ACIDS, EXEMPLIFIED BY A SYNTHESIS OF DIHYDROSOMATOSTATIN
3. A mild procedure for solid phase peptide synthesis: use of fluorenylmethoxycarbonylamino-acids
4. 9-Fluorenylmethoxycarbonyl function, a new base-sensitive amino-protecting group
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