4.7 Article

Photoredox-Catalyzed Hydrosulfonylation of Arylallenes

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 85, Issue 4, Pages 2250-2259

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.9b02960

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Funding

  1. RUDN University Program 5-100
  2. RFBR [18-33-20040]

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(Het)Arylallenes undergo hydrosulfonylation under photoredox-catalyzed conditions. The reaction gives vinyl sulfones in a regio- and diastereoselective manner, employing sodium sulfinates as the sulfonyl source and eosin Y as the photocatalyst. Indol-1-yl, pyrrol-1-yl, phenyl, and naphtylallenes might be used. Aliphatic allenes are incompatible with the reaction conditions.

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