Rice, Scott; Cox, Daniel J.; Marsden, Stephen P.; Nelson, Adam published the artcile< Efficient unified synthesis of diverse bridged polycyclic scaffolds using a complexity-generating 'stitching' annulation approach>, Synthetic Route of 61367-16-6, the main research area is polycyclic compound preparation regioselective diastereoselective; amine arylation cyclization.
Regioselective and stereospecific directed C-H arylation of simple amine substrates e.g., exo-2-aminonorbornane, and cyclisation, delivered three-dimensional scaffolds e.g., (1R,3aR,4R,10bS)-2,3,3a,4,5,10b-hexahydro-1,4-methanobenzo[c]cyclopenta[e]azepin-6(1H)-one. The unified approach significantly expanded the range of bridged ring systems that contain both a nitrogen atom and an aromatic ring.
Chemical Communications (Cambridge, United Kingdom) published new progress about Amines Role: RCT (Reactant), RACT (Reactant or Reagent). 61367-16-6 belongs to class esters-buliding-blocks, and the molecular formula is C8H16ClNO2, Synthetic Route of 61367-16-6.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics