Jersovs, Glebs published the artcileSynthetic Approach toward Enantiopure Cyclic Sulfinamides, Recommanded Product: (S)-2-Methylpropane-2-sulfinamide, the main research area is sulfinamide haloalkenyl diastereoselective cyclization tert butyl cleavage; cyclic sulfinamide asym synthesis oxidation alkylation.
A synthetic approach toward densely substituted enantiopure cyclic sulfinamides possessing up to four consecutive stereogenic centers has been developed based on a completely diastereoselective SN2′ cyclization/tert-Bu cleavage sequence. Diastereospecific transformation of the obtained scaffold into chiral SVI derivatives such as sulfoximines and sulfonimidamides is demonstrated.
Organic Letters published new progress about Bond cleavage. 343338-28-3 belongs to class amides-buliding-blocks, name is (S)-2-Methylpropane-2-sulfinamide, and the molecular formula is C4H11NOS, Recommanded Product: (S)-2-Methylpropane-2-sulfinamide.
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics