Ji, Peng; Zhang, Yueteng; Wei, Yongyi; Huang, He; Hu, Wenbo; Mariano, Patrick A.; Wang, Wei published the artcile< Visible-Light-Mediated, Chemo- and Stereoselective Radical Process for the Synthesis of C-Glyco-amino Acids>, Reference of 4064-06-6, the main research area is homolytic coupling glycoside glycopeptide preparation; stereoselective C glycosylation photoredox catalyzed imine glycopeptide; imino ester chemoselective addition nucleophilic glycosyl radical amino acid.
An approach for efficient synthesis of C-glycosyl amino acids is described. Different from typical photoredox-catalyzed reactions of imines, the new process follows a pathway in which α-imino esters serve as electrophiles in chemoselective addition reactions with nucleophilic glycosyl radicals. The process is highlighted by the mild nature of the reaction conditions, the highly stereoselectivity attending C-C bond formation, and its applicability to C-glycosylations using both armed and disarmed pentose and hexose derivatives
Organic Letters published new progress about Amino acids Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 4064-06-6 belongs to class alcohols-buliding-blocks, and the molecular formula is C12H20O6, Reference of 4064-06-6.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts