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ChemInform Abstract: Nucleosides and Nucleotides. Part 151. Conversion of (Z)-2′-( Cyanomethylene)-2′-deoxyuridines into Their (E)-Isomers via Addition of Thiophenol to the Cyanomethylene Moiety Followed by Oxidative syn- Elimination Reactions.

✍ Scribed by A. E. A. HASSAN; N. NISHIZONO; N. MINAKAWA; S. SHUTO; A. MATSUDA

Publisher
John Wiley and Sons
Year
2010
Weight
38 KB
Volume
28
Category
Article
ISSN
0931-7597

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ChemInform Abstract: Nucleosides and Nuc
ChemInform Abstract: Nucleosides and Nucleotides. Part 156. Chelation-Controlled and Nonchelation-Controlled Diastereofacial Selective Thiophenol Addition Reactions at the 2′-Position of 2′-((Alkoxycarbonyl)methylene)-2′- deoxyuridines: Conversion of (Z)-2′-((Alkoxycarbonyl)methylene)-2′- deoxyuridines into Their (E)-Isomers.
✍ A. E. A. HASSAN; S. SHUTO; A. MATSUDA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Nucleosides and Nucleotides. Part 156. Chelation-Controlled and Nonchelation-Controlled Diastereofacial Selective Thiophenol Addition Reactions at the 2'-Position of 2'-((Alkoxycarbonyl)methylene)-2'-deoxyuridines: Conversion of (Z)-2'-((Alkoxycarbonyl)methylene)-2'-deoxyuridines into Their (E)-Isom