The Synthesis ofC-Methyl Branched-Chain Deoxy Sugar Nucleosides by the Deoxygenative Methylation ofO-Tosylated Adenosines with Grignard Reagents
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/61/7/61_7_2437/_pdf
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1. Deoxygenative [1,2]-Hydride Shift Rearrangements in Nucleoside and Sugar Chemistry: Analogy with the [1,2]-Electron Shift in the Deoxygenation of Ribonucleotides by Ribonucleotide Reductases1;The Journal of Organic Chemistry;2007-10-01
2. Synthesis of the Ribosomal P-Site Substrate CCA-pcb;Organic Letters;2005-12-09
3. One-pot deoxygenative conversion of a ribonucleoside to enaminonucleosides involving 1,2-hydride shift rearrangement;Tetrahedron;1996-03
4. Stereoselective synthesis of C-branched nucleoside analogues;Structure and Chemistry (Part E);1996
5. New synthesis of 3′--substituted-3′-nitromethyl-ribo-thymidines;Tetrahedron;1994-04
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