Theoretical Study on the Mechanism of the Petasis-type Boronic Mannich Reaction of Organoboronic Acids, Amines, andα-Hydroxy Aldehydes

2010 ◽  
Vol 28 (1) ◽  
pp. 41-49 ◽  
Author(s):  
Jingcong Tao ◽  
Shuhua Li
RSC Advances ◽  
2016 ◽  
Vol 6 (38) ◽  
pp. 31861-31870 ◽  
Author(s):  
Amedeo Capobianco ◽  
Antonia Di Mola ◽  
Valentina Intintoli ◽  
Antonio Massa ◽  
Vito Capaccio ◽  
...  

The first asymmetric synthesis of 3-amino-substituted isoindolinones was accomplished via cascade hemiaminal-heterocyclization-intramolecular aza-Mannich reaction of amines and 2-formylbenzonitriles using chiral phase transfer conditions (PTC).


2018 ◽  
Vol 3 (31) ◽  
pp. 8787-8792 ◽  
Author(s):  
Mustafa Hussain ◽  
Jianhui Liu ◽  
Zhipeng Zhang ◽  
Mengwei Hu ◽  
Yang Li ◽  
...  

2020 ◽  
Vol 85 (11) ◽  
pp. 7494-7500
Author(s):  
Sebastián O. Simonetti ◽  
Silvina C. Pellegrinet

2014 ◽  
Vol 16 (8) ◽  
pp. 3999-4008 ◽  
Author(s):  
Sheng-Che Yang ◽  
Timm Lankau ◽  
Chin-Hui Yu

Quantum calculations lead the way to a green version of the versatile Mannich reaction in water catalysed by nornicotine.


2003 ◽  
Vol 2003 (9) ◽  
pp. 580-583 ◽  
Author(s):  
Nityagopal Mondal ◽  
Sannyasi Charan Mandal ◽  
Gourab Kanti Das ◽  
Sarbananda Mukherjee

Ab initio quantum mechanical calculation reveals that the first Mannich reaction in Robinson's tropinone synthesis involves both carbon–carbon bond formation and water elimination, which is followed by tautomerisation and a second Mannich reaction to form the protonated tropinone.


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