JOURNAL ARTICLE

Fast, quantitative nucleoside protection under solvent-free conditions

Nicola GiriCaroline BowenJoseph S. VyleStuart L. James

Year: 2008 Journal:   Green Chemistry Vol: 10 (6)Pages: 627-627   Publisher: Royal Society of Chemistry

Abstract

Persilylation of nucleoside hydroxyls was effected in quantitative yields under solvent-free conditions using a ball mill. In addition, one-pot persilylation and acylation of cytidine was performed as an exemplar reaction demonstrating the utility of solvent-free approaches to nucleoside chemistry.

Keywords:
Nucleoside Acylation Cytidine Chemistry Solvent Organic chemistry Ball mill Combinatorial chemistry Nucleotide Catalysis Chemical engineering Stereochemistry Biochemistry

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50
Cited By
1.83
FWCI (Field Weighted Citation Impact)
17
Refs
0.84
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

Chemical Synthesis and Analysis
Life Sciences →  Biochemistry, Genetics and Molecular Biology →  Molecular Biology
Organoboron and organosilicon chemistry
Physical Sciences →  Chemistry →  Organic Chemistry
Boron Compounds in Chemistry
Health Sciences →  Medicine →  Radiology, Nuclear Medicine and Imaging

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