Piper, Stefan published the artcileDirect aminoalkylation of α-branched aldehydes with in situ generated glycine cation equivalents, Safety of 2-Methyl-3-(3,4-methylenedioxyphenyl)propionaldehyde, the main research area is aminoalkylation aldehyde glycine cation equivalent; butyrolactone amino preparation; aminobutanediol alkyl preparation.
The efficient synthesis of β-formyl-α-aminocarboxylates by direct aminoalkylation of aldehydes with in situ generated ternary iminium salts from inexpensive starting materials is described. These compounds are easily transformed into α-amino-β,β-dialkyl-γ-butyrolactones and α,α-dialkyl-β-dialkylamino-butane-1,4-diols and can be used as versatile building blocks.
Synlett published new progress about Aldehydes Role: RCT (Reactant), RACT (Reactant or Reagent). 1205-17-0 belongs to class isoquinoline, name is 2-Methyl-3-(3,4-methylenedioxyphenyl)propionaldehyde, and the molecular formula is C11H12O3, Safety of 2-Methyl-3-(3,4-methylenedioxyphenyl)propionaldehyde.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem