Boiling water-catalyzed neutral and selective N-Boc deprotection - Chemical Communications (RSC Publishing)
BOC Protection and Deprotection
Deprotection of N-Boc Groups under Continuous-Flow High-Temperature Conditions,The Journal of Organic Chemistry - X-MOL
Deprotection of a primary Boc group under basic conditions - ScienceDirect
tert-Butyloxycarbonyl protecting group - Wikiwand
tert-Butyloxycarbonyl protecting group - Wikipedia
Mild deprotection of the N-tert‐butyloxycarbonyl (N-Boc) group using oxalyl chloride
tert-Butyloxycarbonyl protecting group - Wikipedia
tert-Butoxy carbamate (Boc)protecting group.
How does tertiary butoxycarbonyl act as a protecting group in organic synthesis? - Quora
Protecting groups and deprotection- -OH, -COOH, C=O, -NH2 groups.
Not just another way to remove Boc | amphoteros
Suppression of Side Reactions During Final Deprotection Employing a Strong Acid in Boc Chemistry: Regeneration of Methionyl Residues from Their Sulfonium Salts | SpringerLink
Deprotection of Boc using TAF to obtained free amine group - Chemistry Stack Exchange
Di-tert-butyl dicarbonate - Wikipedia
Boiling water-catalyzed neutral and selective N-Boc deprotection - Chemical Communications (RSC Publishing)
Protecting Groups for Amines: Carbamates – Master Organic Chemistry
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
Protecting Groups for Amines: Carbamates – Master Organic Chemistry
Tertiary-butoxycarbonyl (Boc) – A strategic group for N-protection/ deprotection in the synthesis of various natural/unnatural N-unprotected aminoacid cyanomethyl esters - ScienceDirect
Incomplete Tryptophan Boc Group Removal – Peptide Chemistry Portal
