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Rh(II)-mediated domino [4+1]-annulation of alpha-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes. / Medvedev, Jury J.; Efimov, V.; Shafran, Yuri M. et al.
In: Beilstein Journal of Organic Chemistry, Vol. 13, 30.11.2017, p. 2569-2576.

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

Harvard

Medvedev, JJ, Efimov, V, Shafran, YM, Suslonov, VV, Bakulev, VA & Nikolaev, VA 2017, 'Rh(II)-mediated domino [4+1]-annulation of alpha-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes', Beilstein Journal of Organic Chemistry, vol. 13, pp. 2569-2576. https://doi.org/10.3762/bjoc.13.253

APA

Medvedev, J. J., Efimov, V., Shafran, Y. M., Suslonov, V. V., Bakulev, V. A., & Nikolaev, V. A. (2017). Rh(II)-mediated domino [4+1]-annulation of alpha-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes. Beilstein Journal of Organic Chemistry, 13, 2569-2576. https://doi.org/10.3762/bjoc.13.253

Vancouver

Medvedev JJ, Efimov V, Shafran YM, Suslonov VV, Bakulev VA, Nikolaev VA. Rh(II)-mediated domino [4+1]-annulation of alpha-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes. Beilstein Journal of Organic Chemistry. 2017 Nov 30;13:2569-2576. doi: 10.3762/bjoc.13.253

Author

Medvedev, Jury J. ; Efimov, V. ; Shafran, Yuri M. et al. / Rh(II)-mediated domino [4+1]-annulation of alpha-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes. In: Beilstein Journal of Organic Chemistry. 2017 ; Vol. 13. pp. 2569-2576.

BibTeX

@article{b9124af8d53141e1ad81a198ad0ef0ef,
title = "Rh(II)-mediated domino [4+1]-annulation of alpha-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes",
keywords = "[4+1]-annulation, catalysis, diazo compounds, domino reactions, thiophenes, DIRHODIUM(II,II) TETRAACETATE COMPLEXES, HIGHLY DIASTEREOSELECTIVE SYNTHESIS, FORMAL 4+1 CYCLOADDITION, H INSERTION REACTIONS, DIAZOCARBONYL COMPOUNDS, SULFUR YLIDES, N-H, ENANTIOSELECTIVE CYCLOPROPANATION, STEREOSELECTIVE-SYNTHESIS, THIOCARBONYL YLIDES",
author = "Medvedev, {Jury J.} and V. Efimov and Shafran, {Yuri M.} and Suslonov, {Vitaliy V.} and Bakulev, {Vasiliy A.} and Nikolaev, {Valerij A.}",
year = "2017",
month = nov,
day = "30",
doi = "10.3762/bjoc.13.253",
language = "English",
volume = "13",
pages = "2569--2576",
journal = "Beilstein Journal of Organic Chemistry",
issn = "1860-5397",
publisher = "Beilstein-Institut Zur Forderung der Chemischen Wissenschaften",

}

RIS

TY - JOUR

T1 - Rh(II)-mediated domino [4+1]-annulation of alpha-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes

AU - Medvedev, Jury J.

AU - Efimov, V.

AU - Shafran, Yuri M.

AU - Suslonov, Vitaliy V.

AU - Bakulev, Vasiliy A.

AU - Nikolaev, Valerij A.

PY - 2017/11/30

Y1 - 2017/11/30

KW - [4+1]-annulation

KW - catalysis

KW - diazo compounds

KW - domino reactions

KW - thiophenes

KW - DIRHODIUM(II,II) TETRAACETATE COMPLEXES

KW - HIGHLY DIASTEREOSELECTIVE SYNTHESIS

KW - FORMAL 4+1 CYCLOADDITION

KW - H INSERTION REACTIONS

KW - DIAZOCARBONYL COMPOUNDS

KW - SULFUR YLIDES

KW - N-H

KW - ENANTIOSELECTIVE CYCLOPROPANATION

KW - STEREOSELECTIVE-SYNTHESIS

KW - THIOCARBONYL YLIDES

UR - http://www.scopus.com/inward/record.url?scp=85040463064&partnerID=8YFLogxK

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000416841100002

U2 - 10.3762/bjoc.13.253

DO - 10.3762/bjoc.13.253

M3 - Article

VL - 13

SP - 2569

EP - 2576

JO - Beilstein Journal of Organic Chemistry

JF - Beilstein Journal of Organic Chemistry

SN - 1860-5397

ER -

ID: 6178977