scholarly journals Chirality Conversion of Dipeptides in the Schiff Bases of Binol Aldehydes with Multiple Hydrogen Bond Donors

2009 ◽  
Vol 30 (2) ◽  
pp. 409-414 ◽  
2021 ◽  
pp. 130136
Author(s):  
Addi Dana Sánchez-Pacheco ◽  
Mónica Hernández-Vergara ◽  
Everardo Jaime-Adán ◽  
Simón Hernández-Ortega ◽  
Jesús Valdés-Martínez

2016 ◽  
Vol 12 ◽  
pp. 295-300 ◽  
Author(s):  
Ming-Liang Zhang ◽  
Deng-Feng Yue ◽  
Zhen-Hua Wang ◽  
Yuan Luo ◽  
Xiao-Ying Xu ◽  
...  

For the first time, a catalytic asymmetric Henry reaction of 1H-pyrrole-2,3-diones was achieved with a chiral bifunctional amine-thiourea as a catalyst possessing multiple hydrogen-bond donors. With this developed method, a range of 3-hydroxy-3-nitromethyl-1H-pyrrol-2(3H)-ones bearing quaternary stereocenters were obtained in acceptable yield (up to 75%) and enantioselectivity (up to 73% ee).


2012 ◽  
Vol 1 (5) ◽  
pp. 603-608 ◽  
Author(s):  
Yunhua Chen ◽  
Samuel T. Jones ◽  
Ian Hancox ◽  
Richard Beanland ◽  
Edward J. Tunnah ◽  
...  

2011 ◽  
Vol 356-360 ◽  
pp. 48-51
Author(s):  
Qi Tong ◽  
Ti Feng Jiao

In order to investigate the intermolecular hydrogen bonding of special amphiphiles, two bolaform amphiphilic Schiff bases (GN1 and GN2) with different hydrophilic spacers were designed, and their interaction with barbituric acid were tested by liquid chromatography. The chromatographic properties showed that both the Schiff bases showed hydrogen bonding interaction with barbituric acid. In addition, the influence of various detectors was also studied on both cases. Experimental results show that the test with FLD showed better determination than other detectors. It is proposed that due to the directionality and strong matching of hydrogen bond, one barbituric acid molecule can be encapsulated into the intramolecular area of GN1, while two barbituric acid molecules were trapped into the GN2 molecule through intermolecular H-bonds for GN2 due to the long spacer and flexible structure. A rational complex mode was proposed.


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