SnCl4 versus TiCl4-mediated coupling between N-6-benzoyladenine and perbenzoylated 2-deoxypyranose: Application to the synthesis of certain homochiral acyclo and carboacyclonucleosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. 9-(2-Hydroxyethoxymethyl)guanine activity against viruses of the herpes group
2. Inhibition of S-adenosyl-L-homocysteine hydrolase by the aliphatic nucleoside analogue - 9-(S)-(2,3-dihydroxypropyl)adenine
3. Selective Manipulation of Hydroxy Groups in (2S,3S)-Threitol
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1. Highly Enantioselective Synthesis of Designed Chiral Acyclonucleosides and Acyclonucleotides by Organocatalytic Aza-Michael Addition;Chemistry - A European Journal;2011-03-08
2. ChemInform Abstract: SnCl4- Versus TiCl4-Mediated Coupling Between N-6-Benzoyladenine and Perbenzoylated 2-Deoxypyranose. Application to the Synthesis of Certain Homochiral Acyclo and Carboacyclonucleosides.;ChemInform;2010-08-22
3. Transformation of Glycals into 2,3-Unsaturated Glycosyl Derivatives;Organic Reactions;2003-07-22
4. AMINO-THIOCYANATION OF ELECTRON RICH OLEFINS AS AN EFFICIENT PURINE AND PYRIMIDINE N-ALKYLATION PROCESS;Synthetic Communications;2002
5. Periodate oxidation in chemistry of nucleic acids: Dialdehyde derivatives of nucleosides, nucleotides, and oligonucleotides (Review);Russian Journal of Bioorganic Chemistry;2000-07
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