Weigel, William K. published the artcileSynthesis of amino-diamondoid pharmacophores via photocatalytic C-H aminoalkylation, HPLC of Formula: 343338-28-3, the main research area is amino diamondoid pharmacophore preparation; adamantane imine aminoalkylation photocatalyzed iridium; saxagliptin core rimantadine diastereoselective enantioselective preparation.
A direct C-H aminoalkylation reaction using two light-activated H-atom transfer catalyst systems that enabled the introduction of protected amines to native adamantane scaffolds with C-C bond formation was reported. The scope of adamantane and imine reaction partners was broad and deprotection provided versatile amine and amino acid building blocks. Using readily available chiral imines, the diastereo- and enantioselective synthesis of the saxagliptin core and rimantadine derivatives was also described.
Chemical Communications (Cambridge, United Kingdom) published new progress about Aldimines Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 343338-28-3 belongs to class amides-buliding-blocks, name is (S)-2-Methylpropane-2-sulfinamide, and the molecular formula is C4H11NOS, HPLC of Formula: 343338-28-3.
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics