Arylation of adamantanamines: IX. Copper(I)-catalyzed arylation of adamantane-containing amines


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Abstract

Copper(I)-catalyzed arylation of 14 adamantane-containing amines with iodobenzene, 1-fluoro-4-iodobenzene, 1-iodo-4-(trifluoromethyl)benzene, and 1-iodo-4-methoxybenzene has been studied under the conditions optimized previously. The yields of the N-arylation products have been shown to depend in a complicated manner on the amine structure, steric environment of the amino group, and substituent nature in iodobenzene.

About the authors

A. D. Averin

Faculty of Chemistry; Frumkin Institute of Physical Chemistry and Electrochemistry

Author for correspondence.
Email: averin@org.chem.msu.ru
Russian Federation, Leninskie gory 1, Moscow, 119991; Leninskii pr. 31-4, Moscow, 119071

S. P. Panchenko

Faculty of Chemistry

Email: averin@org.chem.msu.ru
Russian Federation, Leninskie gory 1, Moscow, 119991

A. S. Abel

Faculty of Chemistry

Email: averin@org.chem.msu.ru
Russian Federation, Leninskie gory 1, Moscow, 119991

O. A. Maloshitskaya

Faculty of Chemistry

Email: averin@org.chem.msu.ru
Russian Federation, Leninskie gory 1, Moscow, 119991

G. M. Butov

Volzhskii Polytechnic Institute

Email: averin@org.chem.msu.ru
Russian Federation, ul. Engel’sa 42a, Volzhskii, Volgograd oblast, 404121

E. N. Savelyev

Volgograd State Technical University

Email: averin@org.chem.msu.ru
Russian Federation, pr. imeni Lenina 28, Volgograd, 400005

B. S. Orlinson

Volgograd State Technical University

Email: averin@org.chem.msu.ru
Russian Federation, pr. imeni Lenina 28, Volgograd, 400005

I. A. Novakov

Volgograd State Technical University

Email: averin@org.chem.msu.ru
Russian Federation, pr. imeni Lenina 28, Volgograd, 400005

I. P. Beletskaya

Faculty of Chemistry; Frumkin Institute of Physical Chemistry and Electrochemistry

Email: averin@org.chem.msu.ru
Russian Federation, Leninskie gory 1, Moscow, 119991; Leninskii pr. 31-4, Moscow, 119071

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