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Angewandte Chemie International Edition, ISSN 1433-7851, 02/2019, Volume 58, Issue 9, pp. 2864 - 2869
A method for electrophilic sulfenylation by organophosphorus‐catalyzed deoxygenative O‐atom transfer from sulfonyl chlorides is reported. This C−S bond‐forming... 
organocatalysis | reaction mechanisms | sulfenylation | phosphorus | redox chemistry | Chlorides | Dichloropropane | Catalysis | Perfluoroalkyls | Phosphine | Deoxygenation | Redox properties | Substrates | Phosphine oxide | Sulfenylation | Oxygen Atom Transfer | Redox chemistry | Organocatalysis | Phosphetane
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2016, Volume 113, Issue 10, pp. 2609 - 2614
Journal Article
Angewandte Chemie - International Edition, ISSN 1433-7851, 02/2019, Volume 58, Issue 9, pp. 2864 - 2869
A method for electrophilic sulfenylation by organophosphorus-catalyzed deoxygenative O-atom transfer from sulfonyl chlorides is reported. This C-S bond-forming... 
organocatalysis | reaction mechanisms | sulfenylation | phosphorus | redox chemistry | INTRAMOLECULAR SULFENOAMINATION | OXYGEN-ATOM TRANSFER | TRIFLUOROMETHANESULFONYL CHLORIDE | SULFUR | REGIOSELECTIVE SULFENYLATION | CHEMISTRY, MULTIDISCIPLINARY | INDOLES | ASYMMETRIC OXIDATION | DIRECT TRIFLUOROMETHYLTHIOLATION | BOND | CARBOXYLIC-ACIDS
Journal Article