By the same authors

From the same journal

Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation

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Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation. / Klein, Johannes E. M. N.; Taylor, Richard J. K.

In: European Journal of Organic Chemistry, No. 34, 12.2011, p. 6821-6841.

Research output: Contribution to journalLiterature reviewpeer-review

Harvard

Klein, JEMN & Taylor, RJK 2011, 'Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation', European Journal of Organic Chemistry, no. 34, pp. 6821-6841. https://doi.org/10.1002/ejoc.201100836

APA

Klein, J. E. M. N., & Taylor, R. J. K. (2011). Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation. European Journal of Organic Chemistry, (34), 6821-6841. https://doi.org/10.1002/ejoc.201100836

Vancouver

Klein JEMN, Taylor RJK. Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation. European Journal of Organic Chemistry. 2011 Dec;(34):6821-6841. https://doi.org/10.1002/ejoc.201100836

Author

Klein, Johannes E. M. N. ; Taylor, Richard J. K. / Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation. In: European Journal of Organic Chemistry. 2011 ; No. 34. pp. 6821-6841.

Bibtex - Download

@article{494bd60077e8497dad31e66dffaa71cf,
title = "Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation",
abstract = "This review describes transition-metal-catalysed and -mediated processes for the preparation of oxindoles from anilides through C(3)C(3a) bond formation. Traditional methods, such as the Heck reaction, and recent developments, including direct ArH coupling processes, are presented, as are applications in natural product synthesis.",
author = "Klein, {Johannes E. M. N.} and Taylor, {Richard J. K.}",
year = "2011",
month = dec,
doi = "10.1002/ejoc.201100836",
language = "English",
pages = "6821--6841",
journal = "European Journal of Organic Chemistry",
issn = "1434-193X",
publisher = "Wiley-VCH Verlag",
number = "34",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation

AU - Klein, Johannes E. M. N.

AU - Taylor, Richard J. K.

PY - 2011/12

Y1 - 2011/12

N2 - This review describes transition-metal-catalysed and -mediated processes for the preparation of oxindoles from anilides through C(3)C(3a) bond formation. Traditional methods, such as the Heck reaction, and recent developments, including direct ArH coupling processes, are presented, as are applications in natural product synthesis.

AB - This review describes transition-metal-catalysed and -mediated processes for the preparation of oxindoles from anilides through C(3)C(3a) bond formation. Traditional methods, such as the Heck reaction, and recent developments, including direct ArH coupling processes, are presented, as are applications in natural product synthesis.

UR - http://www.scopus.com/inward/record.url?scp=81855210999&partnerID=8YFLogxK

U2 - 10.1002/ejoc.201100836

DO - 10.1002/ejoc.201100836

M3 - Literature review

SP - 6821

EP - 6841

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

SN - 1434-193X

IS - 34

ER -