187275-91-8Relevant articles and documents
Total synthesis of rutaecarpine and analogues by tandem azido reductive cyclization assisted by microwave irradiation
Kamal, Ahmed,Reddy, M. Kashi,Reddy, T. Srinivasa,Santos, Leonardo Silva,Shankaraiah, Nagula
scheme or table, p. 61 - 64 (2011/02/25)
The total synthesis of rutaecarpine and several analogues has been developed by using an azido reductive cyclization process starting from substituted azido benzoic acids. The intramolecular azido reductive cyclization step was performed with triphenylphosphine or Ni2B in HCl-MeOH (1 M) using microwave irradiation. This synthetic route is amenable for the generation of a library of quinazolinone compounds. Georg Thieme Verlag Stuttgart - New York.
Novel Synthetic Route to Benzopolyazamacrocycles. Synthesis of 16-Membered Tetrabenzotetraazamacrocycles via Bisquinazolinone Annelation and Reductive Ring Enlargement
Eguchi, Shoji,Matsushita, Yuji,Takeuchi, Hisato
, p. 6975 - 6979 (2007/10/02)
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