Ugi reaction with isocyanoindoles / Mironov M.A., Tokareva M.I., Ivantsova M.N., Mokrushin V.S. // Russian Journal of Organic Chemistry. - 2004. - V. 40, l. 6. - P. 847-853.

ISSN:

10704280

Type:

Article

Abstract:

Ugi reaction with 5-isocyanoindoles afforded a number of amino acids, β-lactams, and tetrazoles. The described approach can be applied to combinatorial synthesis of biologically active compounds of the indole series.

Author keywords:

Index keywords:

1 (1 methyl 1h indol 5 yl) 5 (1 methyl 1 morpholinocyclohexyl)tetrazole; 1 (1 methyl 1h indol 5 yl) 5 (1 methyl 1 morpholinoethyl)tetrazole; 5 [1 [2 (1h indol 3 yl)ethylamino] 1 methylcyclohexyl] 1 (1

DOI:

10.1023/B:RUJO.0000044548.0766

Смотреть в Scopus:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-6344229212&doi=10.1023%2fB%3aRUJO.0000044548.07660.3c&partnerID=40&md5=f664b5bd56fa546936cfce9ccfde4a55

Соавторы в МНС:

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Поле	Значение
Link	https://www.scopus.com/inward/record.uri?eid=2-s2.0-6344229212&doi=10.1023%2fB%3aRUJO.0000044548.07660.3c&partnerID=40&md5=f664b5bd56fa546936cfce9ccfde4a55
Affiliations	Ural State Technical University, Ul. Mira 19, Yekaterinburg, 620002 Russia, Russian Federation
References	Edenborough, M.S., Herbert, R.B., (1988) Nat. Prod. Rep., 5, p. 229; Evans, J.R., Napier, E.J., Yates, P., (1976) J. Antibiot., 29, p. 850; Hoppe, I., Schollkopf, U., (1984) Justus Liebigs Ann. Chem., p. 600; Beck, B., Hess, S., Doemling, A., (2000) Bioorg. Med. Chem. Lett., 10, p. 1701; Wentrup, C., Stutz, U., Wollweber, H.-J., (1978) Angew. Chem., 90, p. 731; Mironov, M.A., Kleban, M.I., Mokrushin, V.S., (2001) Mendeleev Commun., p. 114; Ugi, I., Felzer, U., Eholzer, R., (1965) Angew. Chem., 77, p. 492; Johnson, H.E., Crosby, D.G., (1963) J. Org. Chem., 28, p. 2794; Ugi, I., Doemling, A., (2000) Angew. Chem., Int. Ed., 39, p. 3168; Ugi, I., (1962) Angew. Chem., 74, p. 9; Doemling, A., Chi, K.-Z., Barrere, M., (1999) Bioorg. Med. Chem. Lett., 9, p. 2871; Zhang, J., Jacobson, A., Rusche, J.R., Herlihy, W., (1999) J. Org. Chem., 64, p. 1074
Correspondence Address	Ural State Technical University, Ul. Mira 19, Yekaterinburg, 620002 RussiaRussian Federation; email: mir@htf.ustu.ru
Language of Original Document	English
Abbreviated Source Title	Russ. J. Org. Chem.
Source	Scopus