61554-52-7Relevant academic research and scientific papers
Efficient syntheses of 2,3-disubstituted natural quinazolinones via iridium catalysis
Fang, Jie,Zhou, Jianguang
, p. 2389 - 2391 (2012/04/11)
Natural products sclerotigenin, pegamine, deoxyvasicinone, mackinazolinone, and rutaecarpine were synthesized. Core quinazolinone structures were constructed via Ir catalysis. The Royal Society of Chemistry 2012.
Oxygen analogues of the benzodiazepine alkaloids sclerotigenin and circumdatin F
Witt, Anette,Bergman, Jan
, p. 351 - 355 (2007/10/03)
A new type of fused oxazepinones 9a and 9b, which are analogues of sclerotigenin and circumdatin F, were obtained in a two step synthesis from 2-(2-amino-benzoylamino)-benzoic acid or the corresponding methyl ester. Secondly a new synthesis of circumdatin F arose from this work, where 2-(2-propionylaminobenzoylamino)-benzoic acid methyl ester was used as an intermediate.
