Abstract
AbstractAn efficient and simple radical chain reaction to convert terminal alkynes into arenesulfonylmethylcyclopentanes is described. The reaction involves a radical addition–translocation–cyclization process and necessitates solely the use of readily available arenesulfonyl chlorides in tetrahydrofuran. Interestingly, this radical‐mediated C−H activation process took place with a high level of retention of configuration when an enantiomerically pure starting material was used.
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