Campbell, Craig D.; Duguet, Nicolas; Gallagher, Katherine A.; Thomson, Jennifer E.; Lindsay, Anita G.; O’Donoghue, AnnMarie C.; Smith, Andrew D. published the artcile< Tandem multi-step synthesis of C-carboxyazlactones promoted by N-heterocyclic carbenes>, HPLC of Formula: 112-63-0, the main research area is azlactone phenoxycarbonyl preparation; oxazolinone phenoxycarbonyl preparation; amino acid anisoyl tandem cyclization coupling chloroformate carboxyl transfer; carbene heterocyclic catalyst amino acid cascade coupling chloroformate.
Cascade reaction sequences incorporating N-heterocyclic carbene-based organocatalysis have been developed that allow the direct preparation of a range of (±)-4-phenoxycarbonylazlactones I (R1 = 4-MeOC6H4; R2 = Me, n-Bu, i-Bu, PhCH2, 4-PhCH2OC6H4CH2) in good isolated yields (66-84%) from the corresponding racemic N-p-anisoyl amino acids II.
Chemical Communications (Cambridge, United Kingdom) published new progress about Amino acids, acyl Role: RCT (Reactant), RACT (Reactant or Reagent). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, HPLC of Formula: 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics