A convenient method for removal of the t-butyl group from nucleoside bis(t-butyl) phosphates under non-acidic conditions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Di-tert-butylN,N-Diethylphosphoramidite. A New Phosphitylating Agent for the Efficient Phosphorylation of Alcohols
2. Di-t-butyl N, N-diethylphosphoramidite and dibenzyl N, N-diethylphosphoramidite. Highly reactive reagents for the ‘phosphite-triester’ phosphorylation of serine-containing peptides
3. Organophosphorus esters—I
4. Di-t-Butyl Phosphorobromidate. A New Selective Phosphorylating Agent Containing Acid-Labile Protecting Groups
5. A new method for the synthesis of branched oligoribonucleotides using a fully protected branched triribonucleoside diphosphate unit
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2. Protection for the Phosphate Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
3. meta-Chloroperbenzoic acid (mCPBA): a versatile reagent in organic synthesis;RSC Adv.;2014
4. Diruthenium Alkynyl Compounds with Phosphonate Capping Groups;Organometallics;2013-02-05
5. Phosphonate-free phosphorylation of alcohols using bis-(tert-butyl) phosphoramidite with imidazole·hydrochloride and imidazole as the activator;Tetrahedron Letters;2011-07
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