Standard

Ugi Reaction with Isocyanoindoles. / Mironov, M. A.; Tokareva, M. I.; Ivantsova, M. N. et al.
In: Russian Journal of Organic Chemistry, Vol. 40, No. 6, 01.06.2004, p. 847-853.

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

Harvard

Mironov, MA, Tokareva, MI, Ivantsova, MN & Mokrushin, VS 2004, 'Ugi Reaction with Isocyanoindoles', Russian Journal of Organic Chemistry, vol. 40, no. 6, pp. 847-853. https://doi.org/10.1023/B:RUJO.0000044548.07660.3c

APA

Mironov, M. A., Tokareva, M. I., Ivantsova, M. N., & Mokrushin, V. S. (2004). Ugi Reaction with Isocyanoindoles. Russian Journal of Organic Chemistry, 40(6), 847-853. https://doi.org/10.1023/B:RUJO.0000044548.07660.3c

Vancouver

Mironov MA, Tokareva MI, Ivantsova MN, Mokrushin VS. Ugi Reaction with Isocyanoindoles. Russian Journal of Organic Chemistry. 2004 Jun 1;40(6):847-853. doi: 10.1023/B:RUJO.0000044548.07660.3c

Author

Mironov, M. A. ; Tokareva, M. I. ; Ivantsova, M. N. et al. / Ugi Reaction with Isocyanoindoles. In: Russian Journal of Organic Chemistry. 2004 ; Vol. 40, No. 6. pp. 847-853.

BibTeX

@article{c8f34d30cf0e4a828fe61ce443f6fda8,
title = "Ugi Reaction with Isocyanoindoles",
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 = "Mironov, {M. A.} and Tokareva, {M. I.} and Ivantsova, {M. N.} and Mokrushin, {V. S.}",
year = "2004",
month = jun,
day = "1",
doi = "10.1023/B:RUJO.0000044548.07660.3c",
language = "English",
volume = "40",
pages = "847--853",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "6",

}

RIS

TY - JOUR

T1 - Ugi Reaction with Isocyanoindoles

AU - Mironov, M. A.

AU - Tokareva, M. I.

AU - Ivantsova, M. N.

AU - Mokrushin, V. S.

PY - 2004/6/1

Y1 - 2004/6/1

N2 - 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.

AB - 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.

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000224147900015

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=6344229212

U2 - 10.1023/B:RUJO.0000044548.07660.3c

DO - 10.1023/B:RUJO.0000044548.07660.3c

M3 - Article

VL - 40

SP - 847

EP - 853

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 6

ER -

ID: 43815146