Regioselective Introduction of Allylic Groups into the C-2 or C-3 Position of Furanoside Rings
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/19/2/19_2_303/_pdf
Reference10 articles.
1. Formation of convenient chiral intermediates from carbohydrates and their use in synthesis
2. New chiral synthons derived from D-glucose. Synthesis of pyranosides having oxygenated dimethyl branched structures.
3. Synthesis of 9-(3-deoxy-3-C-methyl-β-d-xylofuranosyl)-adenine: a branched-chain sugar analog of cordycepin
4. The use of 1,3-dithiane in a regioselective synthesis of a novel 2-alkyl-2-deoxy-D-arabinofuranose branched-chain sugar
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3. Regioselective Introduction of 2-Propynyl Groups into the C-2 or C-3 Position of Furanoside Ring;Chemistry Letters;1997-06
4. Reaction of 2-Deoxy-2-C-(3-bromoacetoxypropyl)-α-D-arabinofuranosides with Oligonucleotide1;Nucleosides and Nucleotides;1994-12
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