Ugi reaction with isocyanoindoles / Mironov MA,Tokareva MI,Ivantsova MN,Mokrushin VS // RUSSIAN JOURNAL OF ORGANIC CHEMISTRY. - 2004. - V. 40, l. 6. - P. 847-853.

ISSN/EISSN:

1070-4280 / 1608-3393

Type:

Article

Abstract:

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

Author keywords:

ANALOGS

DOI:

10.1023/B:RUJO.0000044548.0766

Web of Science ID:

ISI:000224147900015

Соавторы в МНС:

Другие поля

Поле	Значение
Month	JUN
Publisher	MAIK NAUKA/INTERPERIODICA/SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013-1578 USA
Language	English
EISSN	1608-3393
Keywords-Plus	ANALOGS
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	mir@htf.ustu.ru
ResearcherID-Numbers	Ivantsova, Maria/R-5878-2016
ORCID-Numbers	Ivantsova, Maria/0000-0002-2389-0523
Number-of-Cited-References	12
Usage-Count-Last-180-days	3
Usage-Count-Since-2013	6
Journal-ISO	Russ. J. Organ. Chem.
Doc-Delivery-Number	857VS