Acid-catalysed hydrolysis of methoxy-substituted trityl trifluoroethyl ethers: a kinetic and computational investigation of leaving group effects
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Reference53 articles.
1. Greene's Protective Groups in Organic Synthesis
2. N-Tritylamino Acids and Peptides. A New Method of Peptide Synthesis1
3. Studies on Polynucleotides. V.1 Stepwise Synthesis of Oligonucleotides. Syntheses of Thymidylyl-(5' → 3')-thymidylyl-(5' → 3')-thymidine and Deoxycytidylyl-(5' → 3')-deoxyadenylyl-(5' → 3')-thymidine2
4. Studies on Polynucleotides. XIV.1 Specific Synthesis of the C3″-C5″ Interribonucleotide Linkage. Syntheses of Uridylyl-(3″→5″)-Uridine and Uridylyl-(3″→5″)-Adenosine2
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3. FLP reactivity of [Ph3C]+ and (o-tolyl)3P and the capture of a Staudinger reaction intermediate;Dalton Transactions;2017
4. Acid-catalysed hydrolysis of trityl derivatives in strongly acidic aqueous media;Journal of Physical Organic Chemistry;2013-11-05
5. The triazolyl analogue of the trityl cation;Tetrahedron Letters;2013-08
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