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The ligated boryl radical (LBR) has emerged as a potent tool for activating alkyl halides in radical transformations through halogen-atom transfer (XAT). However, unactivated alkyl chlorides still present an open challenge for this strategy. We herein describe a new activation mode of the LBR for the activation of unactivated alkyl chlorides to construct a C(sp
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Journal of the American Chemical Society
University of Chinese Academy of Sciences
Beijing National Laboratory for Molecular Sciences
Binzhou People's Hospital
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Fang et al. (Thu,) studied this question.