Zahradnik, R„ Electronic Structure

Zahradnik, R., Electronic Structure of Heterocyclic Sulfur Compounds, 5, 1. Zahradnik, R., Koutecky, J., Theoretical Studies of Physico-chemical Properties and Reactivity of Azines, 5, 69. 

Zahradnik, R., Electronic Structure of Heterocyclic Sulfur Compounds, 5,1. 

The other two chapters deal with the application of molecular orbital theory to heterocyclic chemistry. The groups surveyed are (a) sulfur heterocycles and (6) azines. The chapters, which are authored by R. Zahradnik and J. Koutecky, discuss the relevance of theoretical calculation to reactivity, electronic structure, and other physicochemical properties of the compounds. The new techniques of theoretical chemistry have been applied with great success to carbocyclic compounds their significance in heterocyclic chemistry will surely increase. 

Arisawa, M., Ramesh, N.G., Nakajima, M., Tohma, H., and Kita, Y, Hypervalent iodine(lll)-induced intramolecular cychzation of a-(aryl)alkyl-P-dicarbonyl compounds a convenient synthesis of benzarmulated and spirobenzannulated compounds, /. Org. Chem., 66, 59, 2001. Eberson, L., Reaction between organic and metal ion species, in Electron Transfer Reactions in Organic Chemistry, Reactivity and Structure, Vol. 25, Hafner, K., Lehn, J.-M., Rees, C.W., von Rague-Schleyer, R, Trost, B.M., and Zahradnik, R, Eds., Springer-Verlag, Berhn, 1987, chap. 7. Bockman, T.M., ShuMa, D., and Kochi, J.K., Photoinduced electron transfer from enol silyl ethers to quinone. Part 1. Pronounced effects of solvent polarity and added salt on the formation of a-enones, J. Chem. Soc., Perkin Trans. 2, 1623, 1996. 

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