Stevens rearrangement of unsaturated ammonium salts. Synthesis of substituted furans


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Abstract

Ammonium salts bearing but-2-ynyl and phenacyl or 2-(naphth-2-yl)-2-oxoethyl moieties at the nitrogen atom underwent Stevens rearrangement to form substituted furan-3-amines. Quaternization of the latter afforded appropriate iodomethylates.

About the authors

M. O. Manukyan

Institute of Organic Chemistry, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

Author for correspondence.
Email: manukyanmeri@gmail.com
Armenia, pr. Azatutyana 26, Yerevan, 0014

T. A. Sahakyan

Institute of Organic Chemistry, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

Email: manukyanmeri@gmail.com
Armenia, pr. Azatutyana 26, Yerevan, 0014

A. Kh. Gyulnazaryan

Institute of Organic Chemistry, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

Email: manukyanmeri@gmail.com
Armenia, pr. Azatutyana 26, Yerevan, 0014

A. V. Babakhanyan

Abovyan Armenian State Pedagogical University

Email: manukyanmeri@gmail.com
Armenia, Yerevan

N. S. Minasyan

Molecular Structure Research Center, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

Email: manukyanmeri@gmail.com
Armenia, Yerevan

K. S. Barseghyan

Institute of Organic Chemistry, Scientific-Technological Center of Organic and Pharmaceutical Chemistry

Email: manukyanmeri@gmail.com
Armenia, pr. Azatutyana 26, Yerevan, 0014


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