Abstract:
A simple method for pyridoxal structural modification via furan ring closure was developed resulting in 2-acyl- and 2-heteroarylfuro[2,3-c]pyridines. The reaction products can be proposed as pyridoxal mimetics to inhibit pyridoxal 5′-phosphate-dependent enzymes.
Citation:
A. S. Morkovnik, A. A. Zubenko, L. N. Divaeva, V. G. Kartsev, G. S. Borodkin, A. I. Klimenko, “The novel structural modification of pyridoxal via its cyclization into 2-acyl- and 2-heteroarylfuro[2,3-c]pyridines”, Mendeleev Commun., 29:1 (2019), 116–118
Linking options:
https://www.mathnet.ru/eng/mendc1442
https://www.mathnet.ru/eng/mendc/v29/i1/p116
This publication is cited in the following 2 articles:
Aashima Batra, Manpreet Kaur, Deepender Kaushik, Simran Kaur, Madhuri T. Patil, Vinod D. Chaudhari, Subash Chandra Sahoo, Deepak B. Salunke, “Synthesis of Triazolo[4′,5′:4,5]furo[2,3-c]pyridine via Post Modification of an Unusual Groebke–Blackburn–Bienaymé Multicomponent Reaction”, ACS Omega, 9:27 (2024), 29372
A. A. Zubenko, L. N. Divaeva, A. S. Morkovnik, L. N. Fetisov, V. S. Sochnev, K. N. Kononenko, A. N. Bodryakov, A. I. Klimenko, “Structural Modification of Pyridoxal. Synthesis and Evaluation of Anti-Infective Activity of New 4-Chloro- and 4-Alkyl(dialkyl)aminomethyl-2-hetaryl(hetaroyl)furo[2,3-c]pyridines”, Russ J Gen Chem, 90:12 (2020), 2242
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