New radical cascade reaction constructs halogenated spiro compounds, demonstrating broad substrate scope and efficiency.
A new BCB-type substrate to assemble halogenated spiro[cyclobutane-1,3'-quinolin]-2'-one derivatives via a radical cascade strain-release cyclization reaction has been successfully developed. The reaction features broad substrate scope, mild reaction conditions, and separated diastereomers. Importantly, the reaction time is very short (3-5 min), leading to this strategy being highly time-efficient and practical value.
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Liu et al. (2025) studied this question.
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