52358-58-4Relevant articles and documents
An asymmetric synthesis of (+)-erysotramidine
Blake, Alexander J.,Gill, Christopher,Greenhalgh, Daniel A.,Simpkins, Nigel S.,Zhang, Fengzhi
, p. 3287 - 3292 (2005)
A new asymmetric total synthesis of the erythrinan alkaloid erysotramidine is described, which uses chiral base desymmetrisation, N-acyliminium addition, and 6-exo-trig radical cyclisation as the key steps. Georg Thieme Verlag Stuttgart.
Synthesis of the erythrina alkaloid erysotramidine
L'Homme, Chloé,Ménard, Marc-André,Canesi, Sylvain
, p. 8481 - 8485 (2015/03/18)
A concise synthesis of erysotramidine (an alkaloid belonging to the erythrina family) was achieved starting with an inexpensive phenol and amine derivative. The synthesis is based on oxidative phenol dearomatizations mediated by a hypervalent iodine reage
General and efficient strategy for erythrinan and homoerythrinan alkaloids: Syntheses of (±)-3-demethoxyerythratidinone and (±)- erysotramidine
Gao, Shuanhu,Tu, Yong Qiang,Hu, Xiangdong,Wang, Shaohua,Hua, Rongbao,Jiang, Yijun,Zhao, Yuming,Fan, Xiaohui,Zhang, Shuyu
, p. 2373 - 2376 (2007/10/03)
A general and efficient strategy to both aromatic-type and nonaromatic-type erythrinan and homoerythrinan alkaloids has been developed. This approach involves a key two-step sequence, an alkylation of a ketone with various N-substituted iodoacetamides fol