A carbamoyl-protective group for tyrosine that facilitates purification of hydrophobic synthetic peptides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. Solid-phase peptide synthesis: from standard procedures to the synthesis of difficult sequences
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3. Rates of Hydrolysis of Carbamate and Carbonate Esters in Alkaline Solution
4. Question of amide group participation in carbamate hydrolysis
5. Cyclization-activated prodrugs. Basic carbamates of 4-hydroxyanisole
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1. A Helping Hand to Overcome Solubility Challenges in Chemical Protein Synthesis;Journal of the American Chemical Society;2016-09-01
2. The road to the synthesis of “difficult peptides”;Chemical Society Reviews;2016
3. Expedient Total Synthesis of Small to Medium-Sized Membrane Proteins via Fmoc Chemistry;Journal of the American Chemical Society;2014-02-21
4. Protection of the indole nucleus of tryptophan in solid-phase peptide synthesis with a dipeptide that can be cleaved rapidly at physiological pH;Tetrahedron Letters;2011-11
5. A new protecting group for tryptophan in solid-phase peptide synthesis which protects against acid-catalyzed side reactions and facilitates purification by HPLC;Tetrahedron Letters;2009-06
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