范围(计算机科学)
模块化设计
组合化学
计算机科学
双环分子
化学
构造(python库)
基质(水族馆)
双功能
限制
钥匙(锁)
纳米技术
材料科学
有机分子
分子
药物发现
生化工程
脚手架
合成生物学
作者
Jiaxin Xie,William Y Zhao,Johnny Z Wang,William L. Lyon,Noriyuki Takanashi,Alice Long,Taylor Sodano,Christopher B. Kelly,Marian C. Bryan,David W. C. MacMillan
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-01-22
卷期号:391 (6783): 399-406
被引量:3
标识
DOI:10.1126/science.aec5748
摘要
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 2 - and Csp 3 -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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