Protecting group - Wikipedia
Trityl Group - an overview | ScienceDirect Topics
The kinetics and mechanism of the acid-catalysed detritylation of nucleotides in non-aqueous solution - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B816235B
Reduction of cysteine-S-protecting groups by triisopropylsilane. - Abstract - Europe PMC
Key Reactions Of Sugars: Glycosylation and Protection
Glen Report 19.14 - MICROARRAYS, NANOTECHNOLOGY AND BEYOND
SciELO - Brasil - Solid-Phase Peptide Synthesis of Dipeptide (Histidine-β-Alanine) as a Chelating Agent by Using Trityl Chloride Resin, for Removal of Al<sup>3+</sup>, Cu<sup>2+</sup>, Hg<sup>2+</sup> and Pb<sup>2+</sup>: Experimental and Theoretical ...
Molecules | Free Full-Text | Synthesis of Thiol Derivatives of Biological Active Compounds for Nanotechnology Application | HTML
Trityl Group - an overview | ScienceDirect Topics
Trityl Protection in Organic Chemistry
Molecules | Free Full-Text | Synthesis of Thiol Derivatives of Biological Active Compounds for Nanotechnology Application | HTML
Glen Report 13.13 - Trityl Group in the 3rd Millenium:<br> New Perspectives for Oligonucleotide Chemistry and Beyond
LiCl-mediated, easy, and low-cost removal of the trityl group from protected alcohols and diols - ScienceDirect
Trityl Derivative - an overview | ScienceDirect Topics
Protecting group - Wikipedia
Protecting group - Wikipedia
Detritylation - an overview | ScienceDirect Topics
WO2014033466A1 - Method and compositions for removing acid-labile protecting groups - Google Patents
Application of trityl moieties in chemical processes: part I | SpringerLink
A three-component reagent system for rapid and mild removal of O -, N - and S -trityl protecting groups - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00067C
Trityl Derivative - an overview | ScienceDirect Topics
Molecules | Free Full-Text | Synthesis of Thiol Derivatives of Biological Active Compounds for Nanotechnology Application | HTML
Prevention of aspartimide formation during peptide synthesis using cyanosulfurylides as carboxylic acid-protecting groups | Nature Communications
Chemical Forums: TBS, TIPS, Trityl protecting group mechanism
The kinetics and mechanism of the acid-catalysed detritylation of nucleotides in non-aqueous solution - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B816235B
