891782-22-2Relevant academic research and scientific papers
Direct synthesis of chiral aziridines from N-tert-butyl-sulfinylketimines
Morton, Daniel,Pearson, David,Field, Robert A.,Stockman, Robert A.
, p. 1833 - 1835 (2008/03/13)
The direct preparation of a range of variously substituted chiral tert-butylsulfinylketimines was achieved in good yield (41-90%), with relatively rapid reaction times (4-15 hours); their synthetic application was examined through the reaction with the yl
S-chiral sulfinamides as highly enantioselective organocatalysts
Pei, Dong,Wang, Zhouyu,Wei, Siyu,Zhang, Yu,Sun, Jian
, p. 5913 - 5915 (2007/10/03)
(Diagram presented) Easily accessible chiral sulfinamide 2 has been developed as the first highly efficient and enantioselective organocatalyst relying solely on a chiral sulfur center for stereochemical induction. In the presence of 20 mol % of 2, a broa
