Journal
NATURE CHEMISTRY
Volume 9, Issue 9, Pages 868-873Publisher
NATURE PORTFOLIO
DOI: 10.1038/NCHEM.2748
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Funding
- CERCA Programme (Generalitat de Catalunya)
- MINECO (Severo Ochoa Excellence Accreditation) [SEV-2013-0319]
- European Research Council [ERC-2015-CoG 681840 - CATA-LUX]
- Marie Sklodowska-Curie Actions [H2020-MSCA-IF-2014 658980]
- MINECO [CTQ2013-45938-P]
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Chiral iminium ions-generated upon condensation of alpha,beta-unsaturated aldehydes and amine catalysts-are used extensively by chemists to make chiral molecules in enantioenriched form. In contrast, their potential to absorb light and promote stereocontrolled photochemical processes remains unexplored. This is despite the fact that visible-light absorption by iminium ions is a naturally occurring event that triggers the mechanism of vision in higher organisms. Herein we demonstrate that the direct excitation of chiral iminium ions can unlock unconventional reaction pathways, enabling enantioselective catalytic photochemical beta-alkylations of enals that cannot be realized via thermal activation. The chemistry uses readily available alkyl silanes, which are recalcitrant to classical conjugate additions, and occurs under illumination by visible-light-emitting diodes. Crucial to success was the design of a chiral amine catalyst with well-tailored electronic properties that can generate a photo-active iminium ion while providing the source of stereochemical induction. This strategy is expected to offer new opportunities for reaction design in the field of enantioselective catalytic photochemistry.
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