Paper
Regioselective protection of the 2′-hydroxyl group of N-acyl-3′,5′-O-di(t-butyl)silanediylnucleoside derivatives by use of t-BuMgCl and 2-(trimethylsilyl)ethoxymethyl chloride
Published Mar 6, 1995 · T. Wada, M. Tobe, T. Nagayama
Tetrahedron Letters
Q3 SJR score
20
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
Regioselective 2′-O-protection of N-acyl-3′,5′-O-di(t-butyl)silanediylnucleoside derivatives with 2-(trimethylsilyl)ethoxymethyl chloride allows for efficient conversion into
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
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Use of Arabinonucleosides for Development and Implementation of a Novel 2′‐O‐Protecting Group for Efficient Solid‐Phase Synthesis and 2′‐O‐Deprotection of RNA Sequences
A novel 2′-O-protecting group for RNA sequences allows efficient solid-phase synthesis and deprotection without alkylating side-products or mutagenic nucleobase adducts.
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An efficient synthesis of RNA containing GS-441524: the nucleoside precursor of remdesivir
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