Issue 3, 2002
From the journal:

Mendeleev Communications

Formation of cyclopropylazoarenes in the azo coupling reactions of the cyclopropanediazonium ion with active aromatic compounds

Yury V. Tomilov,   Irina V. Kostyuchenko,   Evgeny V. Shulishov  and  Oleg M. Nefedov  

Abstract

The decomposition ofN-cyclopropyl-N-nitrosourea with K 2 CO 3 generates a cyclopropyldiazonium intermediate, which is trappedin situwith 1- and 2-naphthols, 2,7-dihydroxynaphthalene or 8-hydroxyquinoline to afford azo coupling products.

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Article information

DOI
https://doi.org/10.1070/MC2002v012n03ABEH001595
Article type
Paper

Mendeleev Commun., 2002,12, 104-106

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Formation of cyclopropylazoarenes in the azo coupling reactions of the cyclopropanediazonium ion with active aromatic compounds

Y. V. Tomilov, I. V. Kostyuchenko, E. V. Shulishov and O. M. Nefedov, Mendeleev Commun., 2002, 12, 104 DOI: 10.1070/MC2002v012n03ABEH001595

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