Synthesis of pyridinium salts from N-substituted dihydropyridines with BF3OEt2 in the absence of added oxidants
Author:
Funder
Fundação Araucária
CAPES
PRONEX-Carboidratos
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference50 articles.
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1. A strong hydride donating, acid stable and reusable 1,4-dihydropyridine for selective aldimine and aldehyde reductions;Organic & Biomolecular Chemistry;2022
2. 1,4-Dihydropyridine/BF3OEt2 for the reduction of imines: Influences of the amount of added BF3OEt2 and the substitution at N-1 and C-4 of the dihydropyridine ring;Tetrahedron Letters;2019-10
3. Interaction of the Dihydropyridine/Pyridinium Redox Pair Fixed into a V-Shaped Conformation;HETEROCYCLES;2019
4. Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds;Mendeleev Communications;2018-11
5. Pyridinium salts: from synthesis to reactivity and applications;Organic Chemistry Frontiers;2018
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