Remote Substituent Effect Favoring the Formation of syn-Adducts in the Chelation Controlled Radical Reactions of γ-Benzyloxy-α-methylenecarboxylic Acid Esters.

ChemInform ◽  
2003 ◽  
Vol 34 (37) ◽  
Author(s):  
Hajime Nagano ◽  
Hisako Ohkouchi ◽  
Tomoko Yajima
ACS Omega ◽  
2021 ◽  
Vol 6 (4) ◽  
pp. 3227-3231
Author(s):  
Chizuru Kogame-Asahara ◽  
Hitomi Iguchi ◽  
Kenichiro Honda ◽  
Hajime Shigemitsu ◽  
Toshiyuki Kida

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

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