Selective removal of the -butyloxycarbonyl protecting group in the presence of t-butyl and p-methoxybenzyl esters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. t-Butyloxycarbonylamino Acids and Their Use in Peptide Synthesis
2. New Amine-masking Groups for Peptide Synthesis
3. Synthese von Zwischenprodukten für den Aufbau corticotrop wirksamer Polypeptide III. Das Decapeptid H·Ser-Tyr-Ser-Met-Glu-His-Phe-Arg-Try-Gly·OH und einige seiner Derivate
4. Synthese eines Heptapeptides mit starker CRF-Wirkung
5. Cleavage of N-Carbobenzoxy Groups by dry Hydrogen Bromide and Hydrogen Chloride
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1. Removal of acid-labile protecting or anchoring groups in the presence of polyfluorinated alcohol: Application to solid-phase peptide synthesis;Russian Journal of Bioorganic Chemistry;2016-03
2. Preparation and Applications of 4-Methoxybenzyl Esters in Organic Synthesis;Organic Preparations and Procedures International;2016-01-02
3. Synthesis of 12-membered macrocyclic templates and library analogs for PPI;Tetrahedron Letters;2013-06
4. Protection Reactions;Amino Acids, Peptides and Proteins in Organic Chemistry;2011-04-07
5. Solution-Phase Peptide Synthesis;Amino Acids, Peptides and Proteins in Organic Chemistry;2011-01-31
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