1004781-36-5Relevant articles and documents
Ring-fused aminals: catalyst and solvent-free microwave-assisted α-amination of nitrogen heterocycles
Polshettiwar, Vivek,Varma, Rajender S.
, p. 7165 - 7167 (2008)
A high-yield synthesis of ring-fused aminals via microwave (MW)-assisted α-amination of nitrogen heterocycles at 130 °C under solvent- and catalyst-free conditions is described.
α-amination of nitrogen heterocycles: Ring-fused aminals
Zhang, Chen,De, Chandra Kanta,Mal, Rudrajit,Seidel, Daniel
, p. 416 - 417 (2008/09/20)
Aromatic aminoaldehydes react with cyclic amines to produce ring-fused aminals under thermal conditions. This process is applied to two-step syntheses of the quinazolinone alkaloids deoxyvasicinone and rutaecarpine. Copyright