683226-96-2Relevant academic research and scientific papers
Asymmetric thio-Michael/nucleophilic addition domino reaction with chiral N-sulfinimines
Kamimura, Akio,Okawa, Hidenori,Morisaki, Yuki,Ishikawa, Shingo,Uno, Hidemitsu
, p. 3569 - 3572 (2007)
(Chemical Equation Presented) Optically active N-sulfinimines underwent stereoselective Michael/nucleophilic addition domino reaction triggered by magnesium thiolate to give α-phenylthiomethyl-β-(N-sulfinylamino) esters in high diastereomeric excess. The
Synthesis of Sulfinimines by Direct Condensation of Sulfinamides with Aldehydes Using Cs2CO3 as an Activating and Dehydrating Reagent
Higashibayashi, Shuhei,Tohmiya, Hiraku,Mori, Tomonori,Hashimoto, Kimiko,Nakata, Masaya
, p. 457 - 460 (2007/10/03)
Chiral sulfinimines were prepared from chiral sulfinamides and aldehydes in CH2Cl2 in the presence of cesium carbonate as an amine-activating and dehydrating reagent.
