83706-38-1Relevant articles and documents
Efficient copper-catalyzed N-arylation of sulfoximines with aryl iodides and aryl bromides
Sedelmeier, Joerg,Bolm, Carsten
, p. 6904 - 6906 (2005)
Two simple and inexpensive systems for copper-catalyed N-arylations of sulfoximines with aryl bromides and aryl iodides have been developed. Using 10 mol % of a copper(I) salt in combination with 20 mol % of a 1,2-diamine and Cs2CO3 provides N-arylated sulfoximines in high yields. Various functional groups and heteroatoms are tolarated. The method is complementary to the known protocols for N-arylations of sulfoximines, which require stoichiometric quantities of copper salts or cost-intensive palladium/BINAP catalysts.
Preparation and Reactions of Sulfonimidoyl Fluorides
Johnson, Carl R.,Bis, Kostaki G.,Cantillo, Jose H.,Meanwell, Nicholas A.,Reinhard, Michael F. D.,et al.
, p. 1 - 3 (2007/10/02)
Sulfonimidoyl fluorides have been prepared for the first time by treatment of sulfonimidoyl chlorides with various sources of fluoride ion.Sulfonimidoyl chlorides are reduced to sulfinamides with alkyllithium reagents; however, the corresponding fluorides