Palladium-Catalyzed Direct Arylation of 4-Chromanones: Selective Synthesis of Racemic Isoflavanones and 3,3-Diaryl-4-chromanones

2010 ◽  
Vol 2010 (7) ◽  
pp. 1339-1344 ◽  
Author(s):  
Fabio Bellina ◽  
Tiziana Masini ◽  
Renzo Rossi
2020 ◽  
Vol 59 (46) ◽  
pp. 20394-20398
Author(s):  
Ji Yang ◽  
Jiawang Liu ◽  
Yao Ge ◽  
Weiheng Huang ◽  
Helfried Neumann ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1813
Author(s):  
László Kollár ◽  
Ádám Erdélyi ◽  
Haroon Rasheed ◽  
Attila Takács

The aminocarbonylation of various alkenyl and (hetero)aryl iodides was carried out using tropane-based amines of biological importance, such as 8-azabicyclo[3.2.1]octan-3-one (nortropinone) and 3α-hydroxy-8-azabicyclo[3.2.1]octane (nortropine) as N-nucleophile. Using iodoalkenes, the two nucleophiles were selectively converted to the corresponding amide in the presence of Pd(OAc)2/2 PPh3 catalysts. In the presence of several iodo(hetero)arenes, the application of the bidentate Xantphos was necessary to produce the target compounds selectively. The new carboxamides of varied structure, formed in palladium-catalyzed aminocarbonylation reactions, were isolated and fully characterized. In this way, a novel synthetic method has been developed for the producing of N-acylnortropane derivatives of biological importance.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Chendan Zhu ◽  
Yue Zhao ◽  
Di Wang ◽  
Wei-Yin Sun ◽  
Zhuangzhi Shi

ChemInform ◽  
2011 ◽  
Vol 42 (49) ◽  
pp. no-no
Author(s):  
Charles Beromeo Bheeter ◽  
Jitendra K. Bera ◽  
Henri Doucet

ChemInform ◽  
2015 ◽  
Vol 46 (4) ◽  
pp. no-no
Author(s):  
Imen Smari ◽  
Chiraz Youssef ◽  
Kedong Yuan ◽  
Anissa Beladhria ◽  
Hamed Ben Ammar ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 41 (9) ◽  
Author(s):  
Masahiro Miura ◽  
Tetsuya Satoh

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