Microwave promoted reaction of purin-6-yl magnesium halides with aldehydes in dichloromethane at 100 °C
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. The Chemodiversity of Purine as a Constituent of Natural Products
2. Purinergic signaling
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1. Metal-free direct C-6–H alkylation of purines and purine nucleosides enabled by oxidative homolysis of 4-alkyl-1,4-dihydropyridines at room temperature;Organic & Biomolecular Chemistry;2023
2. Regioselective C6–H Hydroxyalkylation of Purines and Purine Nucleosides via α-C–H Functionalization of Alcohols at Room Temperature;Organic Letters;2022-07-01
3. Traceless proton aided regioselective C(sp2)–C(sp2) construction to synthesize C6-acylated purines and purine nucleosides without metal catalysts;Organic Chemistry Frontiers;2022
4. 2‐ and 6‐Purinylmagnesium Halides in Dichloromethane: Scope and New Insights into the Solvent Influence on the C−Mg Bond;European Journal of Organic Chemistry;2021-12-28
5. General Route to Purin-2-ylmagnesium Halides by Metal–Halogen Exchange in Dichloromethane;Synlett;2020-02-10
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