Divergent Mechanisms for the Skeletal Rearrangement and [2+2] Cycloaddition of Enynes Catalyzed by Gold

Chemistry

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https://doi.org/10.1002/anie.200501937
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Divergent Mechanisms for the Skeletal Rearrangement and [2+2] Cycloaddition of Enynes Catalyzed by Gold. / Nieto-Oberhuber, Cristina; López, Salomé; Munoz-Herranz, Maria et al.
In: Angewandte Chemie International Edition, Vol. 44, No. 38, 20.09.2005, p. 6146-6148.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Nieto-Oberhuber, C, López, S, Munoz-Herranz, M, Cárdenas, DJ, Buñuel, E, Nevado, C & Echavarren, AM 2005, 'Divergent Mechanisms for the Skeletal Rearrangement and [2+2] Cycloaddition of Enynes Catalyzed by Gold', Angewandte Chemie International Edition, vol. 44, no. 38, pp. 6146-6148. https://doi.org/10.1002/anie.200501937

APA

Nieto-Oberhuber, C., López, S., Munoz-Herranz, M., Cárdenas, D. J., Buñuel, E., Nevado, C., & Echavarren, A. M. (2005). Divergent Mechanisms for the Skeletal Rearrangement and [2+2] Cycloaddition of Enynes Catalyzed by Gold. Angewandte Chemie International Edition, 44(38), 6146-6148. https://doi.org/10.1002/anie.200501937

Vancouver

Nieto-Oberhuber C, López S, Munoz-Herranz M, Cárdenas DJ, Buñuel E, Nevado C et al. Divergent Mechanisms for the Skeletal Rearrangement and [2+2] Cycloaddition of Enynes Catalyzed by Gold. Angewandte Chemie International Edition. 2005 Sept 20;44(38):6146-6148. doi: 10.1002/anie.200501937

Author

Nieto-Oberhuber, Cristina ; López, Salomé ; Munoz-Herranz, Maria et al. / Divergent Mechanisms for the Skeletal Rearrangement and [2+2] Cycloaddition of Enynes Catalyzed by Gold. In: Angewandte Chemie International Edition. 2005 ; Vol. 44, No. 38. pp. 6146-6148.

Bibtex

@article{6f9d182c0c3049e2989c5fd5351401c5,

title = "Divergent Mechanisms for the Skeletal Rearrangement and [2+2] Cycloaddition of Enynes Catalyzed by Gold",

abstract = "Support for the direct route: That cyclobutenes are not necessary intermediates in the skeletal rearrangement of enynes is supported by DFT calculations and kinetic studies. Cyclobutenes may arise from the corresponding syn-cyclopropylgold(I) carbenes",

author = "Cristina Nieto-Oberhuber and Salom{\'e} L{\'o}pez and Maria Munoz-Herranz and C{\'a}rdenas, {Diego J.} and Elena Bu{\~n}uel and Cristina Nevado and Echavarren, {Antonio M.}",

year = "2005",

month = sep,

day = "20",

doi = "10.1002/anie.200501937",

language = "English",

volume = "44",

pages = "6146--6148",

journal = "Angewandte Chemie International Edition",

issn = "1433-7851",

publisher = "Wiley-VCH Verlag",

number = "38",

}

RIS

TY - JOUR

T1 - Divergent Mechanisms for the Skeletal Rearrangement and [2+2] Cycloaddition of Enynes Catalyzed by Gold

AU - Nieto-Oberhuber, Cristina

AU - López, Salomé

AU - Munoz-Herranz, Maria

AU - Cárdenas, Diego J.

AU - Buñuel, Elena

AU - Nevado, Cristina

AU - Echavarren, Antonio M.

PY - 2005/9/20

Y1 - 2005/9/20

N2 - Support for the direct route: That cyclobutenes are not necessary intermediates in the skeletal rearrangement of enynes is supported by DFT calculations and kinetic studies. Cyclobutenes may arise from the corresponding syn-cyclopropylgold(I) carbenes

AB - Support for the direct route: That cyclobutenes are not necessary intermediates in the skeletal rearrangement of enynes is supported by DFT calculations and kinetic studies. Cyclobutenes may arise from the corresponding syn-cyclopropylgold(I) carbenes

U2 - 10.1002/anie.200501937

DO - 10.1002/anie.200501937

M3 - Journal article

VL - 44

SP - 6146

EP - 6148

JO - Angewandte Chemie International Edition

JF - Angewandte Chemie International Edition

SN - 1433-7851

IS - 38

ER -

Research

Text available via DOI: