Theoretical prediction of proton and electron affinities, gas phase basicities, and ionization energies of sulfinamides
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
http://link.springer.com/content/pdf/10.1007/s11224-019-01401-1.pdf
Reference37 articles.
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2. Mancheno OG, Bolm C (2007) Synthesis of sulfonimidamides from sulfinamides by oxidation with N-chlorosuccinimide. Beilstein J Org Chem 3:25
3. Sehgelmeble F, Janson J, Ray C, Rosqvist S, Gustavsson S, Nilsson LI, Minidis A, Holenz J, Rotticci D, Lundkvist J, Arvidsson PI (2012) Sulfonimidamides as sulfonamides bioisosteres: rational evaluation through synthetic, in vitro, and in vivo studies with g-secretase inhibitors. Chem Med Chem 7:396
4. Dinr P, Sadhukhan A, Blomkvist B (2014) Chiral sulfinamides as highly enantioselective organocatalysts. ChemCatChem 6:3063
5. Chelouan A, Recio R, Borrego LG, Alvarez E, Khiar N, Fernandez I (2016) Sulfinamide phosphinates as chiral catalysts for the enantioselective organocatalytic reduction of imines. Org Lett 18:3258
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