Synthesis of pyrazole C-nucleosides via Tin(IV) chloride-promoted reactions of β-d-ribofuranosyl cyanide with β-dicarbonyl compounds
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Metal-catalysed carbon—carbon bond formation in the reaction of β-dicarbonyls with nitriles
2. A new and efficient route to the synthesis of pyrazole and pyrimidine C-nucleoside derivatives
3. A new route to the synthesis of pyrazole and pyrimidine C-nucleoside derivatives
4. Synthesis of ribosyl and arabinosyl cyanides by reaction of 1-O-acyl sugars with trimethylsilyl cyanide
5. A facile preparation of o-acelated β-d-ribofuranosyl cyanide, an important intermediate of c-nucleoside synthesis
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1. One-Pot Synthesis of Aryl PyrazoleC-Nucleoside Analogs of Pyrazofurin from Sugar Alkynes;European Journal of Organic Chemistry;2017-03-17
2. Synthesis of β-enaminodicarbonyl derivatives in the titanium(iv) chloride-promoted reactions of β-dicarbonyl compounds with nitriles;RSC Adv.;2014
3. Nucleosides Modified at the Base Moiety;Chemical Synthesis of Nucleoside Analogues;2013-02-15
4. Unexpected Cyclization During the Mitsunobu Reaction of d-Talose Derivatives;Synlett;2013-01-29
5. A regio- and stereo-controlled approach to triazoloquinoxalinyl C-nucleosides;Carbohydrate Research;2010-11
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