Direct Minisci-Type C–H Amidation of Purine Bases
Author:
Affiliation:
1. Institute of Chemical Sciences, Heriot-Watt University, Edinburgh, EH14 4AS Scotland, U.K.
2. Early Chemical Development, Pharmaceutical Sciences, R&D BioPharmaceuticals, AstraZeneca, Macclesfield, SK10 2NA England, U.K.
Funder
AstraZeneca
Engineering and Physical Sciences Research Council
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03206
Reference54 articles.
1. The Chemodiversity of Purine as a Constituent of Natural Products
2. Recent Advances in Minisci‐Type Reactions
3. Radical Route for the Alkylation of Purine Nucleosides at C6 via Minisci Reaction
4. Silver-Catalyzed Direct C6-H Arylation of Purines and Purine Nucleosides with Arylboronic Acids
5. Metal-, Photocatalyst-, and Light-Free Minisci C–H Alkylation of N-Heteroarenes with Oxalates
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