7-Azabicyclo[2.2.1]heptadienes in electrophilic chalcogenation reactions


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Resumo

Reactions of electrophilic chalcogenation (sulfenylation and selenenylation) of 7-azabicyclo[2.2.1]heptadiene derivatives with electron-withdrawing substituents at the nitrogen atom and the double bond were found to proceed trans-stereospecifically with the formation of 1,2-addition products, resulting from the exo-attack by the electrophile. In the case of 2-tosyl-7-azanorbornadiene, the reaction is regiospecific: the electrophilic species exclusively adds to the carbon atom at position 6. A comparative analysis of the behavior of dimethyl bicyclo-[2.2.1]heptadiene-2,3-dicarboxylate and its 7-aza analogs in the AdE reactions was carried out.

Sobre autores

A. Gavrilova

Department of Chemistry, M. V. Lomonosov Moscow State University

Autor responsável pela correspondência
Email: augava@gmail.com
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

M. Nechaev

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: augava@gmail.com
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

D. Aparshov

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: augava@gmail.com
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

S. Arkhipenko

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: augava@gmail.com
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

R. Antipin

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: augava@gmail.com
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

O. Bondarenko

Department of Chemistry, M. V. Lomonosov Moscow State University

Email: augava@gmail.com
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991

N. Zyk

Department of Chemistry, M. V. Lomonosov Moscow State University; Institute of Physiologically Active Compounds, Russian Academy of Sciences

Email: augava@gmail.com
Rússia, Build. 3, 1 Leninskie Gory, Moscow, 119991; 1 Severnyi proezd, Chernogolovka, Moscow Region, 142432

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