36679-08-0Relevant articles and documents
Efficient syntheses of (±)-cherylline and latifine dimethyl ether
Kumar, A. Sanjeev,Ghosh, Samir,Soundararajan,Mehta
experimental part, p. 1588 - 1594 (2010/07/04)
A concise route for the syntheses of (±)-cherylline and latifine dimethyl ether is reported. The key steps involved are Michael addition of veratrole with p-methoxy nitrostyrene (for cherylline), anisole with 2,3-dimethoxy nitrostyrene (for latifine), and reduction of nitro intermediate, followed by Pictet-Spengler cyclization. Copyright
An efficient synthesis of (+/-) cherylline dimethyl ether
Kumar, A. Sanjeev,Ghosh, Samir,Bhima, Kale,Mehta
experimental part, p. 482 - 484 (2010/02/28)
A concise route for the synthesis of (+/-) cherylline dimethyl ether is reported. The key steps involved are Grignard reaction, conversion of alcohol to nitrile using (N-(p-toluene sulfonyl)imidazole and sodium cyanide), reduction of the nitrile intermedi
Synthesis of 4-aryltetrahydroisoquinolines: Application to the synthesis of cherylline
Ruchirawat, Somsak,Tontoolarug, Sopchok,Sahakitpichan, Poolsar
, p. 635 - 640 (2007/10/03)
A concise route for the synthesis of 4-aryltetrahydroisoquinolines was developed using the addition of Grignard reagents to nitrostyrene derivatives as the key step. The application to the synthesis of cherylline was described.