Methoxycarbonylation of substituted benzenes. Effect of the electronic configuration of carbon radicals in homolytic substitutions
M Fiorentino, L Testaferri, M Tiecco…
Index: Fiorentino,M. et al. Journal of Organic Chemistry, 1976 , vol. 41, p. 173 - 175
Full Text: HTML
Citation Number: 7
Abstract
From studies of relative rates and isomer distributions in homolytic substitutions it emerged that one of the factors affecting the polar nature of carbon-centered radicals is the hybridization of the orbital carrying the unpaired electron; because the s orbital has higher electronegativity than the p orbital, it can be expected that the greater the s character of an orbital, the greater will be its electronegativity and hence the lower will be the ...
Related Articles:
[Cheng, Jiang; Wang, Feng; Xu, Jian-Hua; Pan, Yi; Zhang, Zhaoguo Tetrahedron Letters, 2003 , vol. 44, # 37 p. 7095 - 7098]
[Hajipour, Abdol R.; Rafiee, Fatemeh; Najafi, Narges Applied Organometallic Chemistry, 2014 , vol. 28, # 4 p. 217 - 220]
[Sapountzis, Ioannis; Lin, Wenwei; Kofink, Christiane C.; Despotopoulou, Christina; Knochel, Paul Angewandte Chemie - International Edition, 2005 , vol. 44, # 11 p. 1654 - 1657]
[Yoshikai, Naohiko; Matsumoto, Arimasa; Norinder, Jakob; Nakamura, Eiichi Angewandte Chemie, International Edition, 2009 , vol. 48, # 16 p. 2925 - 2928]
[Shah, Dipen; Kaur, Harjinder Journal of Molecular Catalysis A: Chemical, 2012 , vol. 359, p. 69 - 73]