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Hydrodeoxygenation of sulfoxides to sulfides by a Pt and MoO x co-loaded TiO2 catalyst. Abeda Sultana Touchy, S. M. A. Hakim Siddiki, Wataru Onodera, Kenichi Kon, Ken-ichi Shimizu , Green Chem. , 2016 , 18 , 2554

Synthesis of phenothiazines from cyclohexanones and 2-aminobenzenethiols under transition-metal-free conditions. Yunfeng Liao, Pengcheng Jiang, Shanping Chen, Fuhong Xiao, Guo-Jun Deng , RSC Adv. , 2013 , 3 , 18605

Base-controlled divergent synthesis of vinyl sulfones from (benzylsulfonyl)benzenes and paraformaldehyde. Fuhong Xiao, Yangling Hu, Huawen Huang, Fen Xu, Guo-Jun Deng , Org. Biomol. Chem. , 2020 , 18 , 3527

Does intermolecular SO⋯H–C–SO hydrogen bonding in sulfoxides and sulfones provide a robust supramolecular synthon in the solid state?. Nicolas Brondel, Eamonn J. A. Moynihan, K. Niamh Lehane, Kevin S. Eccles, Curtis J. Elcoate, Simon J. Coles, Simon E. Lawrence, Anita R. Maguire , CrystEngComm , 2010 , 12 , 2910

Benzyl anion transfer in the fragmentation of N-(phenylsulfonyl)-benzeneacetamides: a gas-phase intramolecular SNAr reaction. Shanshan Shen, Yunfeng Chai, Yaqin Liu, Chang Li, Yuanjiang Pan , Org. Biomol. Chem. , 2015 , 13 , 10205

Aza-Knoevenagel-type condensation of secondary amides: direct access to N-monosubstituted β,β-difunctionalized enamines. Pei-Qiang Huang, Wei Ou, Jian-Liang Ye , Org. Chem. Front. , 2015 , 2 , 1094

Oxidation of α-sulfonyl selenides: Formation of selenolesters. Jae Sang Yi, Kyongtae Kim , J. Chem. Soc., Perkin Trans. 1 , 1999 , 71

Acceptorless dehydrogenative coupling reactions with alcohols over heterogeneous catalysts. S. M. A. Hakim Siddiki, Takashi Toyao, Ken-ichi Shimizu , Green Chem. , 2018 , 20 , 2933

Nickel(ii)-catalyzed direct olefination of benzyl alcohols with sulfones with the liberation of H2. Vinod G. Landge, Vinita Yadav, Murugan Subaramanian, Pragya Dangarh, Ekambaram Balaraman , Chem. Commun. , 2019 , 55 , 6130

Palladium-catalyzed asymmetric allylic alkylation (AAA) with alkyl sulfones as nucleophiles. Barry M. Trost, Zhiwei Jiao, Hadi Gholami , Chem. Sci. , 2021 , 12 , 10532