Abstract:
The reaction of 2-alkyl-substituted 5-, 6- and 7-membered cyclic imines with a-bromo ketones in the presence of Hünig's base affords 2,3-dihydro-1H-pyrrolizines, 5,6,7,8-tetrahydroindolizines and 6,7,8,9-tetrahydro-5H-pyrrolo[1,2-a]azepines, respectively.
Bibliographic databases:
Document Type:
Article
Language: English
Citation:
O. I. Shmatova, V. G. Nenajdenko, “Synthesis of azacycloalkane-1,2-fused pyrroles via alkylation of cyclic ketimines with α-bromo ketones”, Mendeleev Commun., 28:3 (2018), 270–271
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https://www.mathnet.ru/eng/mendc1734
https://www.mathnet.ru/eng/mendc/v28/i3/p270
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