Couple-close: Unified approach to semisaturated cyclic scaffolds

Couple-close as a synthetic paradigm has the potential to change the way that synthetic organic chemists approach cyclic scaffold construction. One class of cyclic molecules that has been increasingly sought after is semisaturated cyclic scaffolds, whose specific blend of Csp<sup>2</sup>- and Csp<sup>3</sup>-hybridized components confers distinct properties to these species. However, existing methods to construct these scaffolds are limited, often relying on arene saturation or annulations that require lengthy de novo syntheses. Herein, we describe a unified and highly modular couple-close strategy for the synthesis of semisaturated scaffolds. This approach installs bifunctional linkers onto aromatic rings through a range of bond-forming reactions, and subsequent cyclization furnishes semisaturated bicyclic adducts. Key to this approach is a mechanistically distinct cobalt-catalyzed dehydrogenative radical cyclization that proceeds efficiently even on electronically unbiased arenes, enabling a broad substrate scope under mild reaction conditions.

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Publication Details

Journal
Science
Published
2026-01-22
DOI
https://doi.org/10.1126/science.aec5748
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
22.95
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article

Couple-close: Unified approach to semisaturated cyclic scaffolds

Noriyuki Takanashi, Jiaxin Xie, William L. Lyon, Taylor Sodano et al.
1 citations
Science
Radical Photochemical Reactions
22.95
article

Couple-close: Unified approach to semisaturated cyclic scaffolds

Noriyuki Takanashi, Jiaxin Xie, William L. Lyon, Taylor Sodano, Christopher B. Kelly, Marian C. Bryan, Alice Long, William Y Zhao, Johnny Z Wang, David W C MacMillan
article en
1 citations

Abstract

Couple-close as a synthetic paradigm has the potential to change the way that synthetic organic chemists approach cyclic scaffold construction. One class of cyclic molecules that has been increasingly sought after is semisaturated cyclic scaffolds, whose specific blend of Csp<sup>2</sup>- and Csp<sup>3</sup>-hybridized components confers distinct properties to these species. However, existing methods to construct these scaffolds are limited, often relying on arene saturation or annulations that require lengthy de novo syntheses. Herein, we describe a unified and highly modular couple-close strategy for the synthesis of semisaturated scaffolds. This approach installs bifunctional linkers onto aromatic rings through a range of bond-forming reactions, and subsequent cyclization furnishes semisaturated bicyclic adducts. Key to this approach is a mechanistically distinct cobalt-catalyzed dehydrogenative radical cyclization that proceeds efficiently even on electronically unbiased arenes, enabling a broad substrate scope under mild reaction conditions.

ScienceVol. 391(6783)
Johnson & Johnson (United States) (US), Princeton University (US)
Openalex Percentile: Top 2%
Radical Photochemical Reactions
22.95
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