Institute of Organic Chemistry, Faculty of Chemistry and Pharmacy, University of Regensburg, D-93040 Regensburg, Germany.
J Am Chem Soc. 2020 Apr 22;142(16):7524-7531. doi: 10.1021/jacs.0c00629. Epub 2020 Apr 13.
The combination of photoredox catalysis with the Wolff-Kishner (WK) reaction allows the difunctionalization of carbonyl groups by a radical-carbanion relay sequence (photo-Wolff-Kishner reaction). Photoredox initiated radical addition to -sulfonylhydrazones yields α-functionalized carbanions following the WK-type mechanism. With sulfur-centered radicals, the carbanions are further functionalized by reaction with electrophiles including CO and aldehydes, whereas CF radical addition furnishes a wide range of -difluoroalkenes through β-fluoride elimination of the generated α-CF carbanions. More than 80 substrate examples demonstrate the broad applicability of this reaction sequence. A series of investigations including radical inhibition, deuterium labeling, fluorescence quenching, cyclic voltammetry, and control experiments support the proposed radical-carbanion relay mechanism.
光氧化还原催化与沃尔夫-基希纳(WK)反应相结合,可以通过自由基-碳负离子接力序列(光-Wolff-Kishner 反应)对羰基进行双官能化。光氧化还原引发的-亚磺酰腙的自由基加成反应遵循 WK 型机制,生成α-功能化的碳负离子。带有硫中心的自由基可以通过与包括 CO 和醛在内的亲电试剂进一步反应,对碳负离子进行官能化,而 CF 自由基加成则通过生成的α-CF 碳负离子的β-氟化物消除,生成广泛的-二氟烯烃。超过 80 个底物实例证明了该反应序列的广泛适用性。一系列包括自由基抑制、氘标记、荧光猝灭、循环伏安法和对照实验在内的研究支持所提出的自由基-碳负离子接力机制。