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New catalytic system for the synthesis of imidazo[1,2-a]pyridines by the Ugi reaction. / Mironov, M.; Tokareva, M.; Ivantsova, M. et al.
In: Russian Chemical Bulletin, Vol. 55, No. 10, 2006, p. 1835-1839.

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@article{a24cd993f89b4598899043c88c71c656,
title = "New catalytic system for the synthesis of imidazo[1,2-a]pyridines by the Ugi reaction",
abstract = "A combination of N-hydroxysuccinimide and p-toluenesulfonic acid is proposed as an efficient catalyst for the preparation of a great variety of imidazo[1,2-a]pyridine derivatives by three-component condensation of aromatic isocyanides, aldehydes, and 2-aminopyridine. The advantages of this procedure are high yields of the target products and the absence of side reactions. {\textcopyright} 2006 Springer Science+Business Media, Inc.",
author = "M. Mironov and M. Tokareva and M. Ivantsova and V. Mokrushin",
year = "2006",
doi = "10.1007/s11172-006-0494-6",
language = "English",
volume = "55",
pages = "1835--1839",
journal = "Russian Chemical Bulletin",
issn = "1066-5285",
publisher = "Springer",
number = "10",

}

RIS

TY - JOUR

T1 - New catalytic system for the synthesis of imidazo[1,2-a]pyridines by the Ugi reaction

AU - Mironov, M.

AU - Tokareva, M.

AU - Ivantsova, M.

AU - Mokrushin, V.

PY - 2006

Y1 - 2006

N2 - A combination of N-hydroxysuccinimide and p-toluenesulfonic acid is proposed as an efficient catalyst for the preparation of a great variety of imidazo[1,2-a]pyridine derivatives by three-component condensation of aromatic isocyanides, aldehydes, and 2-aminopyridine. The advantages of this procedure are high yields of the target products and the absence of side reactions. © 2006 Springer Science+Business Media, Inc.

AB - A combination of N-hydroxysuccinimide and p-toluenesulfonic acid is proposed as an efficient catalyst for the preparation of a great variety of imidazo[1,2-a]pyridine derivatives by three-component condensation of aromatic isocyanides, aldehydes, and 2-aminopyridine. The advantages of this procedure are high yields of the target products and the absence of side reactions. © 2006 Springer Science+Business Media, Inc.

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000245091400019

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=33947103093

U2 - 10.1007/s11172-006-0494-6

DO - 10.1007/s11172-006-0494-6

M3 - Article

VL - 55

SP - 1835

EP - 1839

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 10

ER -

ID: 42251228