Protecting groups and deprotection- -OH, -COOH, C=O, -NH2 groups.
tert-Butyloxycarbonyl protecting group - Wikipedia
Mild deprotection of the N-tert‐butyloxycarbonyl (N-Boc) group using oxalyl chloride
Solid-Phase Peptide Synthesis of Dipeptide (Histidine-β-Alanine) as a Chelating Agent by Using Trityl Chloride Resin, for Removal of Al3+, Cu2+, Hg2+ and Pb2+: Experimental and Theoretical Study
Boiling water-catalyzed neutral and selective N -Boc deprotection - Chemical Communications (RSC Publishing) DOI:10.1039/B910239F
Protecting Groups for Amines: Carbamates – Master Organic Chemistry
Mild deprotection of the N-tert -butyloxycarbonyl ( N -Boc) group using oxalyl chloride - RSC Advances (RSC Publishing) DOI:10.1039/D0RA04110F
A practical, catalytic and selective deprotection of a Boc group in N,N′-diprotected amines using iron(iii)-catalysis
Protecting Groups for Amines: Carbamates – Master Organic Chemistry
tert-Butyloxycarbonyl protecting group - Wikipedia
Deprotection of Boc using TAF to obtained free amine group - Chemistry Stack Exchange
Amine Protection / Deprotection
boc protection mechanism - ZoneAlarm Results
Deprotection of N-Boc group in ball mill a . | Download Table
PDF) Iodine-Mediated Neutral and Selective N-Boc Deprotection
Not just another way to remove Boc | amphoteros
Deprotection of N-Boc group present in amino acids and other derivatives a | Download Table
Incomplete Tryptophan Boc Group Removal – Peptide Chemistry Portal
Deprotection of a primary Boc group under basic conditions - ScienceDirect
Boc-Protected Amino Groups
Di-tert-butyl dicarbonate - Wikipedia
Protecting Groups for Amines: Carbamates – Master Organic Chemistry
Rapid, effective deprotection of tert-butoxycarbonyl (Boc) amino acids and peptides at high temperatures using a thermally stabl
US20120157563A1 - Water soluble solid phase peptide synthesis - Google Patents
Deprotection of a primary Boc group under basic conditions - ScienceDirect
PDF) Solvent-Free Mechanochemical Deprotection of N -Boc Group
