Nucleophile-assisted cyclization of β-propargylamino acrylic compounds catalyzed by gold(I): a rapid construction of multisubstituted tetrahydropyridines and their fused derivatives

0534628 - ÚOCHB 2021 RIV GB eng J - Článek v odborném periodiku
Matouš, P. - Kadaník, M. - Timoracký, M. - Kuneš, J. - Maříková, J. - Růžička, A. - Kočovský, Pavel - Pour, M.
Nucleophile-assisted cyclization of β-propargylamino acrylic compounds catalyzed by gold(I): a rapid construction of multisubstituted tetrahydropyridines and their fused derivatives.
Organic Chemistry Frontiers. Roč. 7, č. 21 (2020), s. 3356-3367. ISSN 2052-4129. E-ISSN 2052-4129
Institucionální podpora: RVO:61388963
Klíčová slova: vinyl ether * Claisen rearrangement * gold(I)-catalyzed synthesis
Obor OECD: Organic chemistry
Impakt faktor: 5.281, rok: 2020
Způsob publikování: Omezený přístup
https://doi.org/10.1039/D0QO00653J

Au(I)-catalyzed cyclization of β-propargylamino acrylic derivatives 1, carried out in the presence of methanol, afforded tetrahydropyridines 3 in high isolated yields. An intramolecular version, using substrates with pending OH, NHBoc and 3-MeOC6H4 groups as internal O-, N-, and C-nucleophiles, yielded the ortho-fused cyclic derivatives, namely furo[2,3-b]pyridine derivative 14, pyrrolo[2,3-b]pyridine 18, and an unusual chromeno[3,4-c]pyridine 22 with a new quaternary carbon center. Synthetic utilization of the tetrahydropyridines 3 has been demonstrated by their conversion into substances with privileged pharmacophore scaffold. Thus, four 4-aryl piperidine derivatives 23a,b,f,g were obtained on catalytic hydrogenation of the representative 4-aryl tetrahydropyridines 3a,b,f,g, furthermore, the Diels–Alder cycloaddition of dimethyl acetylene dicarboxylate (DMAD) to dienes 3r–3u, possessing a masked dendralene framework, afforded tetrahydroisoquinolines 25r–25u that can be aromatized to produce polysubstituted isoquinolines, as demonstrated by the conversion of 25r into 27r. These domino transformations thus offer numerous variations of this methodology and reveal its potential for synthetic applications.
Trvalý link: http://hdl.handle.net/11104/0313457