Mikołajczyk, M.; Gajl, M.; Błaszczyk, J.; Cypryk, M.; Gostyński, B.
Nucleophilic Substitution at Tetracoordinate Sulfur. Kinetics and Mechanism of the Chloride-Chloride Exchange Reaction in Arenesulfonyl Chlorides: Counterintuitive Acceleration of Substitution at Sulfonyl Sulfur by ortho-Alkyl Groups and Its Origin. Molecules 2020, 25, 1428.
https://doi.org/10.3390/molecules25061428
AMA Style
Mikołajczyk M, Gajl M, Błaszczyk J, Cypryk M, Gostyński B.
Nucleophilic Substitution at Tetracoordinate Sulfur. Kinetics and Mechanism of the Chloride-Chloride Exchange Reaction in Arenesulfonyl Chlorides: Counterintuitive Acceleration of Substitution at Sulfonyl Sulfur by ortho-Alkyl Groups and Its Origin. Molecules. 2020; 25(6):1428.
https://doi.org/10.3390/molecules25061428
Chicago/Turabian Style
Mikołajczyk, Marian, Monika Gajl, Jarosław Błaszczyk, Marek Cypryk, and Bartłomiej Gostyński.
2020. "Nucleophilic Substitution at Tetracoordinate Sulfur. Kinetics and Mechanism of the Chloride-Chloride Exchange Reaction in Arenesulfonyl Chlorides: Counterintuitive Acceleration of Substitution at Sulfonyl Sulfur by ortho-Alkyl Groups and Its Origin" Molecules 25, no. 6: 1428.
https://doi.org/10.3390/molecules25061428
APA Style
Mikołajczyk, M., Gajl, M., Błaszczyk, J., Cypryk, M., & Gostyński, B.
(2020). Nucleophilic Substitution at Tetracoordinate Sulfur. Kinetics and Mechanism of the Chloride-Chloride Exchange Reaction in Arenesulfonyl Chlorides: Counterintuitive Acceleration of Substitution at Sulfonyl Sulfur by ortho-Alkyl Groups and Its Origin. Molecules, 25(6), 1428.
https://doi.org/10.3390/molecules25061428