Formation of Condensed 1H-Pyrrol-2-ylphosphonates and 1,2-Dihydropyridin-2-ylphosphonates via Kabachnik–Fields Reaction of Acetylenic Aldehydes and Subsequent 5-exo-dig or 6-endo-dig Cyclizations
2014
Bukšnaitienė, Rita | Urbanaitė, Aurelija | Čikotienė, Inga
Kabachnik–Fields reactions of various carbocyclic or heterocyclic acetylenic aldehydes together with subsequent Lewis acid catalyzed cyclizations have been studied. It was found that 5-exo-dig versus 6-endo-dig cyclization mode strongly depends on the structure of starting materials. Thus, nonaromatic acetylenic α-anilinomethylphosphonates underwent gold(III)-catalyzed or iodine-mediated 5-exo-dig cyclization to 1H-pyrrol-2-ylphosphonates. In contrast, electron-withdrawing heteroaromatic substrates formed 1,2-dihydropyridin-2-ylphosphonate ring containing materials via an exclusive 6-endo-dig ring-closure process. The dual mode of cyclization is possible only for α-amino (2-alkynylphenyl)methylphosphonates containing a benzene ring .
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