130423-49-3Relevant academic research and scientific papers
Total Synthesis of (+)-Mesembrine Applying Asymmetric Gold Catalysis
Spittler, Michael,Lutsenko, Kiril,Czekelius, Constantin
, p. 6100 - 6105 (2016)
The total synthesis of enantiomerically pure (+)-mesembrine is described. The central pyrrolidine moiety incorporating a quaternary, all-carbon-substituted stereocenter was constructed employing an asymmetric gold-catalyzed cycloisomerization of a 1,4-diynamide.
Oxidative aromatic C-O bond formation: synthesis of 3-functionalized benzo[b]furans by FeCl3-mediated ring closure of a-Aryl ketones
Liang, Zhidan,Hou, Weizhe,Du, Yunfei,Zhang, Yongliang,Pan, Yan,Mao, Deng,Zhao, Kang
supporting information; experimental part, p. 4978 - 4981 (2010/01/16)
A variety of 3-functionalized benzo[b]furans were achieved by way of a FeCl3-medlated Intramolecular cyclization of electron-rich a-aryl ketones. The alkoxy substituent on the benzene ring In the substrates was essential for an efficient cyclization to occur. This novel method allows the construction of benzo[b]furan rings by joining the O-atom on the side chain to the benzene ring via direct oxidative aromatic C-O bond formation.
SYNTHESIS OF FUNCTIONALLY SUBSTITUTED BENZOPYRYLIUM SALTS
Nikolyukin, Yu. A.,Bogza, S. L.,Dulenko, V. I.
, p. 397 - 402 (2007/10/02)
Benzopyrylium salts that contain an acetyl, cyano, or ethoxycarbonyl group in the 4 position of the pyrylium ring were synthesized by the reaction of 3-(3,4-dimethoxyphenyl)pentane-2,4-dione and α-(3,4-dimethoxyphenyl)acetoacetonitrile and ethyl α-(3,4
