1412911-99-9Relevant academic research and scientific papers
Selective synthesis of 5,6-dihydrophenanthridines, 5,6-dihydrobenzo[c][1,8] naphthyridines and their fully aromatized analogues via the Pictet-Spengler reaction mediated by peptide coupling agent propylphosphonic anhydride (T3P)
Augustine, John Kallikat,Alagarsamy, Padma,Jothi, Anandh,Bombrun, Agnes
, p. 6280 - 6287,8 (2012/12/11)
A new method has been developed for the selective synthesis of 5,6-dihydrophenanthridines, 5,6-dihydrobenzo[ c][1,8]naphthyridines and their fully aromatized analogues via the Pictet-Spengler reaction mediated by propylphosphonic anhydride (T3P). The method, which uses less toxic and readily available T3P, generally seems to be more flexible, efficient in the preparation of 5,6-dihydrophenanthridine derivatives and complementary to conventional routes in the preparation of fused pyridines.
Selective synthesis of 5,6-dihydrophenanthridines, 5,6-dihydrobenzo[c][1,8] naphthyridines and their fully aromatized analogues via the Pictet-Spengler reaction mediated by peptide coupling agent propylphosphonic anhydride (T3P)
Augustine, John Kallikat,Bombrun, Agnes,Alagarsamy, Padma,Jothi, Anandh
, p. 6280 - 6287 (2013/01/14)
A new method has been developed for the selective synthesis of 5,6-dihydrophenanthridines, 5,6-dihydrobenzo[ c][1,8]naphthyridines and their fully aromatized analogues via the Pictet-Spengler reaction mediated by propylphosphonic anhydride (T3P). The meth
