组合化学
光催化
构造(python库)
基质(水族馆)
表面改性
反应性(心理学)
化学
纳米技术
计算机科学
组分(热力学)
简单(哲学)
催化作用
反应条件
光催化
材料科学
分子
光学(聚焦)
底物特异性
作者
Vinjamuri Srinivasu,Ajmeera Balaraju,Pratap Mondal,Devarajulu Sureshkumar
标识
DOI:10.1021/acs.joc.5c02434
摘要
Bicyclo[1.1.0]butanes have attracted significant attention from synthetic chemists for their strain-release functionalization, enabling access to complex molecular architectures. This study demonstrates a photocatalyzed, strain-release-driven radical cyclization for efficiently synthesizing heteroarylated spirocyclobutyl oxindoles. By strategically incorporating redox-active functionalities into the substrate design, we achieve an unusual/reverse mode of reactivity in bicyclo[1.1.0]butanes (BCB). This approach enables the broad and efficient installation of diverse heterocycles onto spirocyclobutyl oxindoles under mild, operationally simple conditions, making it suitable for the late-stage functionalization of drug-like molecules.
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