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Abstract
A photoredox strategy to access β-sulfonated cyclopentanones from the reaction of vinyl cyclobutanols with sulfonyl chlorides is described. This reaction employs the inexpensive and easily accessible sulfonyl chlorides as a sulfonyl radical source. The present synthetic protocol is a convenient way to prepare β-sulfonated cyclopentanones.
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Additional information
Funding
This research was supported by Soonchunhyang University Research Fund and Basic Science Research Program through the National Research Foundation of Korea [NRF-2019R1F1A1059821].
