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Nucleoside synthesis by alkylation with 2′,3′,5′-tri-O-benzoyl-D-ribofuranosyl trifiate

✍ Scribed by Robert L. Shone


Book ID
104243926
Publisher
Elsevier Science
Year
1977
Tongue
French
Weight
229 KB
Volume
18
Category
Article
ISSN
0040-4039

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✦ Synopsis


The use of derivatives of trifluorometbylsulfonic acid in synthesis has been explored by several investigators.1'2 Trifluoromethylsulfohates ("triflates")3 in particular have been utilized as exceptionally reactive alkylatihg agents.

4 The use of triflates in carbohydrate5

and nucleosideb synthesis has also recently been noted. We wish to report the utility of 2',3',5'-tri-C-benzoyl-D-ribofuranosyl triflate, II, for nucleoside synthesis.


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Nucleosides LXXXI. An approach to the sy
✍ Hiroshi Ohrui; Jack J. Fox 📂 Article 📅 1973 🏛 Elsevier Science 🌐 French ⚖ 203 KB

In recent years a new class of naturally-occurring nucleosides containing the unusual C-ribosyl linkage ("C-nucleosides") has been discovered 2,3 . Several synthetic routes directed to C-nucleosides have been reported 3-a . Recently, Hanessian and Pernet 9 reported the successful