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Two ways of cyclization 5-imidazolylthioureas with dimethylacetyl endicarboxylate. / Eltsov, Oleg S.; Morzherin, Yuri Yu.; Belskaia, Natalia P. и др.
в: Arkivoc, Том 2008, № 17, 2008, стр. 306-317.

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@article{99cbf62ed2f54d839528a5f02c85bc13,
title = "Two ways of cyclization 5-imidazolylthioureas with dimethylacetyl endicarboxylate",
abstract = "Two ways of cyclization of imidazolyl derivatives of thiourea with dimethylacetylene dicarboxylate (DMAD) were studied. Reaction of N,N'-disubstituted thioureas with DMAD led to formation of a thiazoline ring whereas transformation of trisubstituted thioureas under the same conditions give the novel imidazo[1,5-c][1,3,5]thiadiazine heterocyclic system.",
author = "Eltsov, {Oleg S.} and Morzherin, {Yuri Yu.} and Belskaia, {Natalia P.} and Mokrushin, {Vladimir S.}",
year = "2008",
doi = "10.3998/ark.5550190.0009.h29",
language = "English",
volume = "2008",
pages = "306--317",
journal = "Arkivoc",
issn = "1551-7004",
publisher = "ARKAT USA, Inc.",
number = "17",

}

RIS

TY - JOUR

T1 - Two ways of cyclization 5-imidazolylthioureas with dimethylacetyl endicarboxylate

AU - Eltsov, Oleg S.

AU - Morzherin, Yuri Yu.

AU - Belskaia, Natalia P.

AU - Mokrushin, Vladimir S.

PY - 2008

Y1 - 2008

N2 - Two ways of cyclization of imidazolyl derivatives of thiourea with dimethylacetylene dicarboxylate (DMAD) were studied. Reaction of N,N'-disubstituted thioureas with DMAD led to formation of a thiazoline ring whereas transformation of trisubstituted thioureas under the same conditions give the novel imidazo[1,5-c][1,3,5]thiadiazine heterocyclic system.

AB - Two ways of cyclization of imidazolyl derivatives of thiourea with dimethylacetylene dicarboxylate (DMAD) were studied. Reaction of N,N'-disubstituted thioureas with DMAD led to formation of a thiazoline ring whereas transformation of trisubstituted thioureas under the same conditions give the novel imidazo[1,5-c][1,3,5]thiadiazine heterocyclic system.

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000265191300030

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=79961240250

U2 - 10.3998/ark.5550190.0009.h29

DO - 10.3998/ark.5550190.0009.h29

M3 - Article

VL - 2008

SP - 306

EP - 317

JO - Arkivoc

JF - Arkivoc

SN - 1551-7004

IS - 17

ER -

ID: 38651308