Pharande, Shrikant G. published the artcileMechanochemical IMCR and IMCR-post transformation domino strategies: Towards the sustainable DOS of dipeptide-like and heterocyclic peptidomimetics, HPLC of Formula: 86-51-1, the main research area is privileged heterocyclic peptidomimetic diversity oriented synthesis dipeptide diketopiperazine lactam; mechanochem domino strategy solvent catalyst column free green chem; isocyanide amine carboxylic acid aldehyde Ugi reaction IMCR SCCF.
A facile mechanochem. Ugi four-component reaction (MC-Ugi-4CR) has been developed for the synthesis of new dipeptide-like products in high yields under solvent-, catalyst-, column-free (SCCF) conditions at room temperature in only three minutes. The scope and versatility of this efficient isocyanide-based multicomponent reaction (IMCR) is demonstrated with the first one-pot diversity-oriented synthesis (DOS) of privileged heterocyclic peptidomimetics (PHPs) such as tri-substituted 2,5-diketopiperazines (DKPs) and α,β-unsaturated-γ-lactams via a sustainable mechanochem. domino strategy that includes IMCR-post transformations in high overall yields and in a total reaction time of only six minutes.
New Journal of Chemistry published new progress about Aldehydes Role: RCT (Reactant), RACT (Reactant or Reagent). 86-51-1 belongs to class isoquinoline, name is 2,3-Dimethoxybenzaldehyde, and the molecular formula is C9H10O3, HPLC of Formula: 86-51-1.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem