Mild Hydroalkylation of Terminal Olefins Via Decatungstate/Thiol Cooperative Photocatalysis

Here we report the use of a tetrabutylammonium decatungstate (TBADT)/thiol photocatalytic system for selective addition of acetone and other simple ketone, nitrile, and chlorocarbon functionalities to terminal olefins. This system avoids the use of energetic reagents such as peroxides and proceeds under mild conditions using Earth-abundant element catalysts, providing a sustainable approach to C-C bond formation using activated olefins. Initial exploration reveals that hydroalkylation of unactivated olefins is also possible, though in lower efficiency, and preliminary mechanistic experiments are consistent with a radical mechanism.

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Publication Details

Journal
Organic Letters
Published
2025-04-24
DOI
https://doi.org/10.1021/acs.orglett.5c01088
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.87

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article

Mild Hydroalkylation of Terminal Olefins Via Decatungstate/Thiol Cooperative Photocatalysis

Julian G. West, Austin J. Moser, S. A. Cruz, Peter Sutter et al.
2 citations
Organic Letters
Catalytic C–H Functionalization Methods
1.87
article

Mild Hydroalkylation of Terminal Olefins Via Decatungstate/Thiol Cooperative Photocatalysis

Julian G. West, Austin J. Moser, S. A. Cruz, Peter Sutter, Alex M. Chavez
article en
2 citations

Abstract

Here we report the use of a tetrabutylammonium decatungstate (TBADT)/thiol photocatalytic system for selective addition of acetone and other simple ketone, nitrile, and chlorocarbon functionalities to terminal olefins. This system avoids the use of energetic reagents such as peroxides and proceeds under mild conditions using Earth-abundant element catalysts, providing a sustainable approach to C-C bond formation using activated olefins. Initial exploration reveals that hydroalkylation of unactivated olefins is also possible, though in lower efficiency, and preliminary mechanistic experiments are consistent with a radical mechanism.

Organic LettersVol. 27(17)
Rice University (US)
Welch Foundation, Cancer Prevention and Research Institute of Texas, National Institute of General Medical Sciences, Division of Chemistry
Zero hunger
Openalex Percentile: Top 16%
Catalytic C–H Functionalization Methods
1.87
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