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May 9, 2026Journal of the American Chemical Society2 citationsOpen Access

Cobalt-Catalyzed Highly Regioselective Alkoxycarbonylation of Olefins Driven by Light

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YPYong PengXTXinxin TianZCZhusong Cao

Key Points

  • This research aims to develop a cobalt-catalyzed process for the alkoxycarbonylation of olefins that enhances regioselectivity.
  • Cobalt-catalyzed approach using light to promote reactions under mild conditions.
  • Focus on converting propylene and various linear olefins to terminal esters.
  • Utilization of control experiments and DFT computations to analyze the reaction mechanism.
  • Achieved over 90% regioselectivity for terminal esters from propylene and linear olefins.
  • Demonstrated efficacy in the presence of a wide range of alcohols.
  • Control experiments confirmed the role of light in maintaining the concentration of HCo(CO) species.

Abstract

Alkoxycarbonylation of olefins is a pivotal transformation in the production of esters; however, attaining high regioselectivity in this transformation, specifically using industrially relevant aliphatic olefins, remains a formidable challenge. To date, this objective has been achieved exclusively through the integration of precious Pd catalysts and costly phosphine ligands in a pressurized CO environment at high temperatures. In this study, we present a novel cobalt-catalyzed light-driven protocol for achieving excellent regioselectivity under mild conditions. Specifically, we demonstrate the efficacy of converting propylene, as well as terminal and internal linear olefins, to the corresponding terminal esters with over 90% regioselectivity, accompanied by a wide range of alcohols. Control experiments and DFT computations reveal that light promotes the formation and maintains the concentration of the key species HCo(CO)

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Cite This Study

Peng et al. (2026) studied this question.

synapsesocial.com/papers/69fed153b9154b0b828788c7https://doi.org/10.1021/jacs.5c22182
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