1354-81-0Relevant articles and documents
Bioinspired total synthesis of montanine-type amaryllidaceae alkaloids
Bao, Xu,Cao, Ye-Xing,Chu, Wen-Dao,Qu, Hu,Du, Ji-Yuan,Zhao, Xian-He,Ma, Xiao-Yan,Wang, Cheng-Tao,Fan, Chun-An
, p. 14167 - 14172 (2014/01/06)
Finding a common path: A synthetic strategy inspired by the proposed biogenesis of the montanine-type alkaloids enabled the concise asymmetric synthesis of these compounds in a divergent fashion on the basis of an unprecedented tandem oxidative dearomatization/intramolecular aza-Michael addition as the key step. This bioinspired approach revealed a chemical connection between the cherylline- and montanine-type alkaloids (see scheme). Copyright
Synthesis of aza bicyclic enones via anionic cyclization: Application to the total synthesis of (-)-brunsvigine
Sha, Chin-Kang,Hong, An-Wei,Huang, Chien-Ming
, p. 2177 - 2179 (2007/10/03)
(Matrix presented) A general approach to the synthesis of aza bicyclic enones was developed via a simple two-step annulation involving a Mitsunobu protocol and anionic cyclization. According to this strategy the total synthesis of (-)-brunsvigine was acco
Total synthesis of montanine-type Amarylliidaceae alkaloids, which possess a 5,11-methanomorphanthridine ring system, through cyclization with sodium bis(2-methoxyethoxy)aluminum hydride: The first stereoselective total syntheses of (±)-montanine, (±)-coc
Ishizaki,Hoshino,Iitaka
, p. 7285 - 7295 (2007/10/02)
-
