D 62 Direct C-C coupling of hetarenes with macrocycles [Text] : доклад, тезисы доклада / O. N. Chupakhin, G. L. Rusinov, D. G. Beresnev, N. A. Itsikson // XVII Менделеевский съезд по общей и прикладной химии, Казань, 21-26 сентября 2003 г. : тез. стенд. докл. - Казань, 2003. - P85 Рубрики: ХИМИЧЕСКИЕ НАУКИ |
D 62 Direct nucleophilic functionalization of C(sp2)–H-bonds in arenes and hetarenes by electrochemical methods [Electronic resource] / A. V. Shchepochkin, O. N. Chupakhin, V. N. Charushin, V. A. Petrosyan // Russian Chemical Reviews. - 2013. - Vol.82, №8. - С. 747-772. - Bibliogr. : p. 770-772 (133 ref.) Рубрики: ХИМИЧЕСКИЕ НАУКИ Кл.слова (ненормированные): NUCLEOPHILIC FUNCTIONALIZATION -- C(sp2)–H-BONDS -- HETARENES Аннотация: The data on the main electrochemical methods and approaches used for the direct functionalization of the C(sp2)–H-bond proceeding via the mechanisms of nucleophilic substitution of hydrogen (SNH-reaction) are classified and summarized. The important features of preparative electrochemical processes are considered. A special emphasis is placed on the synthetic potential of the discussed transformations \\\\expert2\\NBO\\Russian Chemical Reviews\\2013, V.82, N8, p.747.pdf |
O-72 Organolithium compounds in the nucleophilic substitution of hydrogen in arenes and hetarenes [Electronic resource] / I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin, V. N. Charushin // Russian Chemical Reviews. - 2015. - Vol. 84, № 12. - С. 1191-1225. - Bibliogr. : p. 1224-1225 (237 ref.) Рубрики: ХИМИЧЕСКИЕ НАУКИ Кл.слова (ненормированные): NUCLEOPHILIC SUBSTITUTION -- HYDROGEN -- ARENES AND HETARENES Аннотация: The review considers the most typical examples of the direct non-activated non-catalytic C–C bond formation in arenes and their metal complexes activated by electron-withdrawing substituents in the aromatic nucleus and in hetarenes (azines and their N-oxides, porphyrins, etc.) upon the reactions with aliphatic and (hetero)aromatic (hetero)organolithium nucleophiles. Particular attention is given to the direct introduction of nitroxide radicals and (hetero)organic moieties into mono-, di- and triazines and their N-oxides. The influence of the structures of the (hetero)aromatic substrate and the (hetero)organolithium nucleophile on the reaction pathway and rate and on the structure of the reaction product is analyzed. \\\\expert2\\nbo\\Russian Chemical Reviews\\2015, V.84, N12, p. 1191-1225.pdf |