Linguistik Streik Lila trityl deprotection mechanism Wütend werden Härte Erbe
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 Group - an overview | ScienceDirect Topics
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 ...
Stabilities of Trityl‐Protected Substrates: The Wide Mechanistic Spectrum of Trityl Ester Hydrolyses - Horn - 2010 - Chemistry – A European Journal - Wiley Online Library
Application of trityl moieties in chemical processes: part I | SpringerLink
Prevention of aspartimide formation during peptide synthesis using cyanosulfurylides as carboxylic acid-protecting groups | Nature Communications
Molecules | Free Full-Text | Synthesis of Thiol Derivatives of Biological Active Compounds for Nanotechnology Application | HTML
Trityl Group - an overview | ScienceDirect Topics
ATDBio - Solid-phase oligonucleotide synthesis
Protecting group - Wikipedia
Key Reactions Of Sugars: Glycosylation and Protection
Arnold Group Literature Blog: Thorium-ligand multiple bonds via reductive deprotection of a trityl group - Chemical Science (RSC Publishing)
Trityl Derivative - an overview | ScienceDirect Topics
Detritylation - an overview | ScienceDirect Topics
News-Archive 2015 - Thieme Chemistry - Georg Thieme Verlag
WO2014033466A1 - Method and compositions for removing acid-labile protecting groups - Google Patents
Trityl Protection in Organic Chemistry
Trityl Group - an overview | ScienceDirect Topics
Molecules | Free Full-Text | Synthesis of Thiol Derivatives of Biological Active Compounds for Nanotechnology Application | HTML
Detritylation - an overview | ScienceDirect Topics
Glen Report 19.14 - MICROARRAYS, NANOTECHNOLOGY AND BEYOND
The kinetics and mechanism of the acid-catalysed detritylation of nucleotides in non-aqueous solution - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B816235B
LOSARTAN | New Drug Approvals
A three-component reagent system for rapid and mild removal of O-, N- and S- trityl protecting groups - Organic & Biomolecular Chemistry (RSC Publishing)
The kinetics and mechanism of the acid-catalysed detritylation of nucleotides in non-aqueous solution - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B816235B
Selective protection and deprotection of alcohols and amines
Protecting group - Wikipedia
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
Glen Report 13.13 - Trityl Group in the 3rd Millenium:<br> New Perspectives for Oligonucleotide Chemistry and Beyond