Cycloaddition reactions

Cycloadditions are among the most useful tools for organic chemists, enabling them to build carbocyclic and heterocyclic structures. These structures can then be used to develop a broad range of functional materials, including pharmaceuticals, agrochemicals, dyes, and optics. With contributions from an international team of leading experts and pioneers in cycloaddition chemistry, this book brings together and reviews recent advances, trends, and emerging research in the field.

 

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Related publications:

Hamdi, A., Laurent, M.Y., Hémon-Ribaud, A., Mostafa, A.S., Massoud, M.A., Selim, K.B. and Dujardin, G., 2019. 1, 3-Dipolar cycloaddition of vinyloxy quinolines with α-alkoxy carbonyl aldonitrones or cyclic surrogates: A comparative study for an asymmetric access to trans 4-quinolinoxy oxaprolines. Tetrahedron, 75(3), pp.429-440. https://www.sciencedirect.com/science/article/pii/S0040402018314844?via%3Dihub

El-Shafey, H.W., Gomaa, R.M., El-Messery, S.M. and Goda, F.E., 2020. Synthetic approaches, anticancer potential, HSP90 inhibition, multitarget evaluation, molecular modeling and apoptosis mechanistic study of thioquinazolinone skeleton: Promising antibreast cancer agent. Bioorganic Chemistry, 101, p.103987. https://www.sciencedirect.com/science/article/pii/S0045206820312840?via%3Dihub

 Othman, D.I., Selim, K.B., Magda, A.A., Tantawy, A.S., Amen, Y., Shimizu, K., Okauchi, T. and Kitamura, M., 2019. Design, synthesis and anticancer evaluation of new substituted thiophene-quinoline derivatives. Bioorganic & Medicinal Chemistry, 27(19), p.115026. https://www.sciencedirect.com/science/article/pii/S0968089619311496?via%3Dihub

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