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- Silyloxymethanesulfinate as a sulfoxylate equivalent for the modular synthesis of sulfones and sulfonyl derivatives. Dae-Kwon Kim, Hyun-Suk Um, Hoyoon Park, Seonwoo Kim, Jin Choi, Chulbom Lee
, Chem. Sci.
, 2020
, 11
, 13071
- Reactions of methyl viologen and nitrite with thiourea dioxide. New opportunities for an old reductant. Sergei V. Makarov, Evgeny V. Kudrik, Rudi van Eldik, Ekaterina V. Naidenko
, J. Chem. Soc., Dalton Trans.
, 2002
, 4074
- Reactions of bromotrifluoromethane and related halides. Part 12. Transformation of disulfides into perfluoroalkyl sulfides in the presence of sulfoxylate anion radical precursors. Jean-Louis Clavel, Bernard Langlois, Roland Nantermet, Marc Tordeux, Claude Wakselman
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 3371
- ‘Super-reduced’ iron under physiologically-relevant conditions. Augustin Mot, Kis Zoltan, Dimitri A. Svistunenko, Grigore Damian, Radu Silaghi-Dumitrescu, Sergei V. Makarov
, Dalton Trans.
, 2010
, 39
, 1464
- Iron-catalyzed synthesis of arylsulfinates through radical coupling reaction. Weixi Zhang, Meiming Luo
, Chem. Commun.
, 2016
, 52
, 2980
- Kinetics and mechanism of oxidation of super-reduced cobalamin and cobinamide species by thiosulfate, sulfite and dithionite. Ilia A. Dereven'kov, Denis S. Salnikov, Sergei V. Makarov, Gerry R. Boss, Oskar I. Koifman
, Dalton Trans.
, 2013
, 42
, 15307
- Recent trends in the chemistry of sulfur-containing reducing agents. Sergei V. Makarov
, Russ. Chem. Rev.
, 2001
, 70
, 885
- Synthesis of ultra-high molecular weight ABA triblock copolymers via aqueous RAFT-mediated gel polymerisation, end group modification and chain coupling. Vu H. Dao, Neil R. Cameron, Kei Saito
, Polym. Chem.
, 2017
, 8
, 6834
- Sodium dithionite mediated one-pot, tandem chemoselective reduction/cyclization for the synthesis of pyrrole fused N-heterocycles. Joydev K. Laha, Surabhi Panday, Pankaj Gupta, Shiv Raj Seth
, Green Chem.
, 2023
, 25
, 161
- Converting between the oxides of nitrogen using metal–ligand coordination complexes. Andrew J. Timmons, Mark D. Symes
, Chem. Soc. Rev.
, 2015
, 44
, 6708