60315-10-8Relevant articles and documents
Radical-initiated cyclization as a key step for the synthesis of oxoprotoberberine alkaloids
Lee, Chih-Shone,Yu, Tsung-Ching,Luo, Jian-Wen,Cheng, Yen-Yao,Chuang, Che-Ping
scheme or table, p. 4558 - 4562 (2009/12/03)
The oxoprotoberberine alkaloids 1a-d have been synthesized efficiently from the enamide derivatives 2a-d by a radical-initiated cyclization reaction utilizing n-Bu3SnH/AIBN and CuCl. The enamide derivatives 2a-d were prepared from phenylethylam
Studies on the synthesis of heterocyclic compounds. Part 698. An alternative protoberberine synthesis; Total synthesis of (+/-)-xylopinine, (+/-)-schefferine, (+/-)nandinine, (+/-)-corydaline, and (+/-)-thalictricavine.
Kametani,Sugai,Shoji,Honda,Satoh,Fukumoto
, p. 1151 - 1155 (2007/10/04)
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