Issue 3, 2024

Ni-catalyzed regioselective C–C bond formation of 1,1-disubstituted allenes with aldehydes

Abstract

Allenes, despite their structural resemblance to alkenes and alkynes, exhibit unique reactivity due to the orthogonal arrangement of their cumulative π-bonds, making precise allene selectivity an emerging area of interest. Previous studies on Ni-catalyzed coupling reactions between allenes and aldehydes yielded diverse regioselectivities, with nucleophilic and reductive conditions producing different outcomes. In this work, we developed a regioselective method for generating linear products through coupling at the terminal carbon of 1,1-disubstituted allenes using photoredox/Ni-dual catalysis. We achieved the regioselectivity by strategically modifying substrate patterns and the catalytic system employing an unconventional P^N ligand. This work represents a notable advancement in selective catalysis, offering valuable insights into the control of allene reactivity.

Graphical abstract: Ni-catalyzed regioselective C–C bond formation of 1,1-disubstituted allenes with aldehydes

Supplementary files

Article information

Article type
Research Article
Submitted
31 Oct 2023
Accepted
09 Dec 2023
First published
11 Dec 2023

Org. Chem. Front., 2024,11, 816-821

Ni-catalyzed regioselective C–C bond formation of 1,1-disubstituted allenes with aldehydes

S. Kim, J. Kim, S. D. Tambe and E. J. Cho, Org. Chem. Front., 2024, 11, 816 DOI: 10.1039/D3QO01800H

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