1334232-93-7Relevant academic research and scientific papers
A competent pot and atom-efficient synthesis of Betti bases over nanocrystalline MgO involving a modified Mannich type reaction
Karmakar, Bikash,Banerji, Julie
, p. 4957 - 4960 (2011)
A simple, efficient, and eco-friendly method for the synthesis of 1-(α-aminoalkyl) naphthols, the Betti bases, has been carried out over a basic nanocrystalline MgO catalyst in aqueous condition. The method has been applied for the synthesis of a range of compounds with variable functionalities in excellent yield and selectivity.
Metal-free new synthesis of 1,3-naphthoxazines via intramolecular cross dehydrogenative-coupling reaction of 1-(α-aminoalkyl)-2-naphthols using hypervalent iodine(III) reagent
Waghmode, Nitin A.,Kalbandhe, Amit H.,Thorat, Prerana B.,Karade, Nandkishor N.
supporting information, p. 680 - 683 (2016/01/26)
A series of 1-(α-aminoalkyl)-2-naphthols were synthesized via three-component Betti reaction of β-naphthol, aldehyde, and cyclic secondary amine under reflux conditions. The subsequent reactions of 1-(α-aminoalkyl)-2-naphthols with (diacetoxyiodo)benzene
Diastereoselective α-C-H functionalization of aliphatic N-heterocycles: An efficient route to ring fused oxazines
Mahato, Sujit,Haldar, Surajit,Jana, Chandan K.
supporting information, p. 332 - 334 (2014/01/06)
A novel method for direct C-H functionalization of saturated N-heterocycles allowing easy access to synthetically as well as biologically important and structurally diverse ring-fused oxazines is developed. The method is operationally simple and highly di
