Biocatalytic Desymmetrization of Prochiral 3-Aryl and 3-Arylmethyl Glutaramides: Different Remote Substituent Effect on Catalytic Efficiency and Enantioselectivity

2018 ◽  
Vol 360 (23) ◽  
pp. 4594-4603 ◽  
Author(s):  
Yu-Fei Ao ◽  
Li-Bin Zhang ◽  
Qi-Qiang Wang ◽  
De-Xian Wang ◽  
Mei-Xiang Wang
2018 ◽  
Vol 16 (1) ◽  
pp. 79-86
Author(s):  
Aarti Dalal ◽  
Radhika Khanna ◽  
Ramesh C. Kamboj

AbstractThe effect on photochemical transformations of the substituents present remotely from the reaction site in 3-benzyloxy-2-(benzo[b]thiophen-2-yl)-4H-chromen-4-ones has been determined. The structure(s) of the substrates and photoproducts were established by spectroscopic techniques (UV, IR, and NMR). The substituents had profound effects on product yield and distribution. Electron withdrawing groups (EWGs) on the benzenoid moiety of the chromenone nucleus increased the yield of the photoproducts whereas electron donating groups (EDGs) decreased the yield. These results may be attributed to “state switching” of the substituents during excitation.


2003 ◽  
Vol 68 (22) ◽  
pp. 8494-8499 ◽  
Author(s):  
J. Edgar Anderson ◽  
Armin de Meijere ◽  
Sergei I. Kozhushkov ◽  
Lodovico Lunazzi ◽  
Andrea Mazzanti

2003 ◽  
Vol 193 (1-2) ◽  
pp. 89-95 ◽  
Author(s):  
Zhi-Peng Li ◽  
Fang-Yi Tang ◽  
Hua-Dong Xu ◽  
Xin-Yan Wu ◽  
Qi-Lin Zhou ◽  
...  

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