Kurteva, Vanya published the artcileConstrained 1-Phenylethyl Amine Analogues as Chiral Auxiliaries in Stereoselective trans-β-Lactam Formation via Staudinger Cycloaddition, Category: isoquinoline, the main research area is lactam beta constrained phenylethyl preparation stereoselective Staudinger cycloaddition.
The efficiency of enantiomeric 1-aminoindane and 1,2,3,4-tetrahydro-1-naphthylamine as chiral auxiliaries in trans-ss-lactam formation via Staudinger cycloaddition is examined Aromatic aldehydes possessing one, two, or three methoxyl groups are used as imine precursors, and the influence of their number and position on the reaction output is studied. A comparison with the results obtained from 1-phenylethyl and 1-(2-naphthyl)ethylamine-derived imines is performed.
Journal of Heterocyclic Chemistry published new progress about Benzaldehydes 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, Category: isoquinoline.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem