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Facile synthesis of unknown 6,7-dihydrofuro[3,4-c]pyridines and 3,4-diaryloylpyridines from N-homopropargylic β-enaminones
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d4ob01884b.pdf
Date
2025-01-01
Author
Yılmaz, Elif Serel
Kaya, Kerem
Zora, Metin
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In this paper, we have uncovered a new reaction of N-homopropargylic β-enaminones, i.e. N-(4-phenyl-3-butynyl)-β-enaminones. When subjected to a reaction with excess molecular iodine or N-iodosuccinimide in the presence of cesium carbonate, N-homopropargylic β-enaminones afford 6,7-dihydrofuro[3,4-c]pyridines in low to moderate yields. The generation of two new C/O-C bonds during the reaction leads to the construction of unknown heterobicyclic 5,6-fused ring systems. In some reactions, 3,4-diaryloylpyridines are also observed in low yields. During the formation of 3,4-diaryloylpyridines, a new carbonyl (ketone) group is generated. The synthesized 6,7-dihydrofuro[3,4-c]pyridines and 3,4-diaryloylpyridines may be of use in pharmaceutical and medicinal chemistry as new and novel molecular entities and structural leads.
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85216212796&origin=inward
https://hdl.handle.net/11511/113635
Journal
Organic and Biomolecular Chemistry
DOI
https://doi.org/10.1039/d4ob01884b
Collections
Department of Chemistry, Article
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E. S. Yılmaz, K. Kaya, and M. Zora, “Facile synthesis of unknown 6,7-dihydrofuro[3,4-c]pyridines and 3,4-diaryloylpyridines from N-homopropargylic β-enaminones,”
Organic and Biomolecular Chemistry
, pp. 0–0, 2025, Accessed: 00, 2025. [Online]. Available: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85216212796&origin=inward.