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Novel Synthesis of Dihydrothiophene-2,5-diimine Derivatives by the Three-Component Reaction of Isocyanides with Enamines and Arylisothiocyanates. / A. mironov, Maxim; N. ivantsova, Maria; I. tokareva, Maria et al.
In: Heterocycles, Vol. 73, No. 1, 01.01.2007, p. 567-579.

Research output: Contribution to journal › Article › peer-review

Harvard

A. mironov, M, N. ivantsova, M, I. tokareva, M & S. mokrushin, V 2007, 'Novel Synthesis of Dihydrothiophene-2,5-diimine Derivatives by the Three-Component Reaction of Isocyanides with Enamines and Arylisothiocyanates', Heterocycles, vol. 73, no. 1, pp. 567-579. https://doi.org/10.3987/COM-07-S(U)33

APA

A. mironov, M., N. ivantsova, M., I. tokareva, M., & S. mokrushin, V. (2007). Novel Synthesis of Dihydrothiophene-2,5-diimine Derivatives by the Three-Component Reaction of Isocyanides with Enamines and Arylisothiocyanates. Heterocycles, 73(1), 567-579. https://doi.org/10.3987/COM-07-S(U)33

Vancouver

A. mironov M, N. ivantsova M, I. tokareva M, S. mokrushin V. Novel Synthesis of Dihydrothiophene-2,5-diimine Derivatives by the Three-Component Reaction of Isocyanides with Enamines and Arylisothiocyanates. Heterocycles. 2007 Jan 1;73(1):567-579. doi: 10.3987/COM-07-S(U)33

Author

A. mironov, Maxim ; N. ivantsova, Maria ; I. tokareva, Maria et al. / Novel Synthesis of Dihydrothiophene-2,5-diimine Derivatives by the Three-Component Reaction of Isocyanides with Enamines and Arylisothiocyanates. In: Heterocycles. 2007 ; Vol. 73, No. 1. pp. 567-579.

BibTeX

@article{10e535aab86e4c129989e28ab3fc8571,
title = "Novel Synthesis of Dihydrothiophene-2,5-diimine Derivatives by the Three-Component Reaction of Isocyanides with Enamines and Arylisothiocyanates",
abstract = "Abstract - A distribution of the products in the reaction of aryl isothiocyanates with isocyanides and 2,2-dialkylenamines has been studied in details. In range 55-60 C this reaction results in the formation of dihydrothiophene-2,5-diimine derivatives, constitutions of which are proved by an X-ray analysis. In contrast at high temperature (above 110 C) the major products in the present reaction are 2-imino-5-thiopyrrolidones. A one step pathway to dihydrothiophene structure has been elaborated. ",
author = "{A. mironov}, Maxim and {N. ivantsova}, Maria and {I. tokareva}, Maria and {S. mokrushin}, Vladimir",
year = "2007",
month = jan,
day = "1",
doi = "10.3987/COM-07-S(U)33",
language = "English",
volume = "73",
pages = "567--579",
journal = "Heterocycles",
issn = "0385-5414",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Novel Synthesis of Dihydrothiophene-2,5-diimine Derivatives by the Three-Component Reaction of Isocyanides with Enamines and Arylisothiocyanates

AU - A. mironov, Maxim

AU - N. ivantsova, Maria

AU - I. tokareva, Maria

AU - S. mokrushin, Vladimir

PY - 2007/1/1

Y1 - 2007/1/1

N2 - Abstract - A distribution of the products in the reaction of aryl isothiocyanates with isocyanides and 2,2-dialkylenamines has been studied in details. In range 55-60 C this reaction results in the formation of dihydrothiophene-2,5-diimine derivatives, constitutions of which are proved by an X-ray analysis. In contrast at high temperature (above 110 C) the major products in the present reaction are 2-imino-5-thiopyrrolidones. A one step pathway to dihydrothiophene structure has been elaborated.

AB - Abstract - A distribution of the products in the reaction of aryl isothiocyanates with isocyanides and 2,2-dialkylenamines has been studied in details. In range 55-60 C this reaction results in the formation of dihydrothiophene-2,5-diimine derivatives, constitutions of which are proved by an X-ray analysis. In contrast at high temperature (above 110 C) the major products in the present reaction are 2-imino-5-thiopyrrolidones. A one step pathway to dihydrothiophene structure has been elaborated.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=45349086573

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000253154500044

U2 - 10.3987/COM-07-S(U)33

DO - 10.3987/COM-07-S(U)33

M3 - Article

VL - 73

SP - 567

EP - 579

JO - Heterocycles

JF - Heterocycles

SN - 0385-5414

IS - 1

ER -

ID: 42249049