Traceless proton aided regioselective C(sp2)–C(sp2) construction to synthesize C6-acylated purines and purine nucleosides without metal catalysts
Author:
Affiliation:
1. School of Chemistry and Materials Science, Ludong University, Yantai 264025, Shandong, P. R China
2. College of Chemistry and Chemical Engineering, Yantai University, Yantai, 264005, Shandong, P. R. China
Abstract
Funder
Natural Science Foundation of Shandong Province
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00712F
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1. Mang Brand-Name Drugs derived from purines and purine nucleosides, including Famciclovir®, Ticagrelor®, Cangrelor®, Adenoscan®, Zovirax® Tabloid®, Leustatin®, Imuran®, etc. , are searched on the website of US Food and Drug Administration (FDA): https://www.fda.gov/
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3. Purines. V. Reaction of 9-phenyl-9H-purine-6-carbonitrile with nucleophilic reagents.
4. Several Approaches to Cyanide Ion-catalyzed Synthesis of 4-Aroyl-1-phenyl-1H-pyrazolo-[3,4-d]pyrimidines
5. Catalytic Action of Azolium Salts. IX. Synthesis of 6-Aroyl-9H-purines and Their Analogues by Nucleophilic Aroylation Catalyzed by Imidazolium or Benzimidazolium Salt.
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3. Metal‐Free, Light‐Mediated, Site‐Specific, Radical C6−H Alkylation of Purines with Alcohols Intervened by Oxalates without Catalysts;European Journal of Organic Chemistry;2023-02-07
4. Direct Regioselective C-H Cyanation of Purines;Molecules;2023-01-17
5. Regiospecificity C(sp2)–C(sp3) Bond Construction between Purines and Alkenes to Synthesize C6-Alkylpurines and Purine Nucleosides Using O2 as the Oxidant;The Journal of Organic Chemistry;2023-01-12
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