Synthesis of 3-iminoindole derivatives by the reactions of aromatic isocyanides with N,N-dialkylbenzylamines / Mironov M.A., Tokareva M.I., Mokrushin V.S. // Mendeleev Communications. - 2007. - V. 17, l. 6. - P. 354-356.

ISSN:

09599436

Type:

Article

Abstract:

The reaction of N,N-dialkylbenzylamines with aromatic isocyanides leading to 2-dialkylamino-3-aryliminoindole derivatives with the subsequent formation of zwitter ionic indolates has been discovered; the structures of final products have been confirmed by X-ray analysis. © 2007.

Author keywords:

Index keywords:

нет данных

DOI:

10.1016/j.mencom.2007.11.020

Смотреть в Scopus:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-36549060048&doi=10.1016%2fj.mencom.2007.11.020&partnerID=40&md5=d1444d7a747420ba8713d2e0eb87392a

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Поле	Значение
Link	https://www.scopus.com/inward/record.uri?eid=2-s2.0-36549060048&doi=10.1016%2fj.mencom.2007.11.020&partnerID=40&md5=d1444d7a747420ba8713d2e0eb87392a
Affiliations	Department of Technology of Organic Synthesis, Urals State Technical University, 620002 Ekaterinburg, Russian Federation
References	Langer, P., Döring, M., (1998) Synlett, p. 396; Berti, C., Creci, L., Andruzzi, R., Trazza, A., (1986) J. Chem. Soc., Perkin Trans., 1, p. 607; Marchetti, L., Creci, L., Tosi, G., (1970) Gazz. Chim. Ital., 100, p. 770; Chauhan, N.A., Parikh, A.R., (1989) Acta Cienc. Indica, Chem., 15, p. 301; Sannicolo, F., (1983) J. Org. Chem., 48, p. 2924; Eberson, L., (1984) J. Org. Chem., 49, p. 2135; Mironov, M.A., Mokrushin, V.S., (1998) Mendeleev Commun., p. 242; Mironov, M.A., Kleban, M.I., Mokrushin, V.S., (2001) Mendeleev Commun., p. 114; Allen, F.H., Kennard, O., Watson, D.G., Brammer, L., Orpin, A.G., Taylor, R., (1987) J. Chem Soc., Perkin Trans., 2, p. 1;
Correspondence Address	Mironov, M.A.; Department of Technology of Organic Synthesis, Urals State Technical University, 620002 Ekaterinburg, Russian Federation; email: mironov@mail.ustu.ru
CODEN	MENCE
Language of Original Document	English
Abbreviated Source Title	Mendeleev Commun.
Source	Scopus