Molecules
(Aug 2022)
[1,5]-Hydride Shift Triggered <i>N</i>-Dealkylative Cyclization into 2-Oxo-1,2,3,4-tetrahydroquinoline-3-carboxylates via Boronate Complexes
Elvira R. Zaitseva,
Dmitrii S. Ivanov,
Alexander Yu. Smirnov,
Andrey A. Mikhaylov,
Nadezhda S. Baleeva,
Mikhail S. Baranov
Affiliations
Elvira R. Zaitseva
Institute of Bioorganic Chemistry, Russian Academy of Sciences, Miklukho-Maklaya 16/10, 117997 Moscow, Russia
Dmitrii S. Ivanov
Institute of Bioorganic Chemistry, Russian Academy of Sciences, Miklukho-Maklaya 16/10, 117997 Moscow, Russia
Alexander Yu. Smirnov
Institute of Bioorganic Chemistry, Russian Academy of Sciences, Miklukho-Maklaya 16/10, 117997 Moscow, Russia
Andrey A. Mikhaylov
Institute of Bioorganic Chemistry, Russian Academy of Sciences, Miklukho-Maklaya 16/10, 117997 Moscow, Russia
Nadezhda S. Baleeva
Institute of Bioorganic Chemistry, Russian Academy of Sciences, Miklukho-Maklaya 16/10, 117997 Moscow, Russia
Mikhail S. Baranov
Institute of Bioorganic Chemistry, Russian Academy of Sciences, Miklukho-Maklaya 16/10, 117997 Moscow, Russia
DOI
https://doi.org/10.3390/molecules27165270
Journal volume & issue
Vol. 27,
no. 16
p.
5270
Abstract
Read online
A new simple one-pot two-step protocol for the synthesis of 2-oxo-1,2,3,4-tetrahydroquinoline-3-carboxylate from 2-(2-(benzylamino)benzylidene)malonate under the action of BF3·Et2O was developed. It was shown that the reaction proceeds through the formation of a stable iminium intermediate containing a difluoroboryl bridge in the dicarbonyl fragment of the molecule.
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