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Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation

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Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation. / Surry, DS; Su, XB; Fox, DJ et al.
In: Angewandte Chemie International Edition, Vol. 44, No. 12, 11.03.2005, p. 1870-1873.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Surry, DS, Su, XB, Fox, DJ, Franckevicius, V, Macdonald, SJF & Spring, DR 2005, 'Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation', Angewandte Chemie International Edition, vol. 44, no. 12, pp. 1870-1873. https://doi.org/10.1002/anie.200462642

APA

Surry, DS., Su, XB., Fox, DJ., Franckevicius, V., Macdonald, SJF., & Spring, DR. (2005). Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation. Angewandte Chemie International Edition, 44(12), 1870-1873. https://doi.org/10.1002/anie.200462642

Vancouver

Surry DS, Su XB, Fox DJ, Franckevicius V, Macdonald SJF, Spring DR. Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation. Angewandte Chemie International Edition. 2005 Mar 11;44(12):1870-1873. doi: 10.1002/anie.200462642

Author

Surry, DS ; Su, XB ; Fox, DJ et al. / Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation. In: Angewandte Chemie International Edition. 2005 ; Vol. 44, No. 12. pp. 1870-1873.

Bibtex

@article{8665a8b5da2d41d4aa36143121caa5c9,
title = "Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation",
abstract = "A biaryl banquet! Biphenyls with four ortho substituents, heteroaromatic compounds, iodinated biaryls, and medium rings containing biaryls are all readily synthesized by organocuprate oxidation. The utility of this new methodology is illustrated by the efficient synthesis of the medium-ring core of sanguiin H-5 (see scheme).",
keywords = "organocuprates, C-C coupling, oxidation, VINYL CHLORIDES, TEMPLATE, biaryls, medium-ring compounds, ULLMANN COUPLING REACTION, ARYL BOND FORMATION, 1ST SYNTHESIS, FUNCTIONALIZED ARYLMAGNESIUM, CONVENIENT, SYMMETRICAL BIARYLS, FACILE SYNTHESIS, SALICYL ALCOHOL",
author = "DS Surry and XB Su and DJ Fox and Vilius Franckevicius and SJF Macdonald and DR Spring",
year = "2005",
month = mar,
day = "11",
doi = "10.1002/anie.200462642",
language = "English",
volume = "44",
pages = "1870--1873",
journal = "Angewandte Chemie International Edition",
issn = "1433-7851",
publisher = "Wiley-VCH Verlag",
number = "12",

}

RIS

TY - JOUR

T1 - Synthesis of medium-ring and iodinated biaryl compounds by organocuprate oxidation

AU - Surry, DS

AU - Su, XB

AU - Fox, DJ

AU - Franckevicius, Vilius

AU - Macdonald, SJF

AU - Spring, DR

PY - 2005/3/11

Y1 - 2005/3/11

N2 - A biaryl banquet! Biphenyls with four ortho substituents, heteroaromatic compounds, iodinated biaryls, and medium rings containing biaryls are all readily synthesized by organocuprate oxidation. The utility of this new methodology is illustrated by the efficient synthesis of the medium-ring core of sanguiin H-5 (see scheme).

AB - A biaryl banquet! Biphenyls with four ortho substituents, heteroaromatic compounds, iodinated biaryls, and medium rings containing biaryls are all readily synthesized by organocuprate oxidation. The utility of this new methodology is illustrated by the efficient synthesis of the medium-ring core of sanguiin H-5 (see scheme).

KW - organocuprates

KW - C-C coupling

KW - oxidation

KW - VINYL CHLORIDES

KW - TEMPLATE

KW - biaryls

KW - medium-ring compounds

KW - ULLMANN COUPLING REACTION

KW - ARYL BOND FORMATION

KW - 1ST SYNTHESIS

KW - FUNCTIONALIZED ARYLMAGNESIUM

KW - CONVENIENT

KW - SYMMETRICAL BIARYLS

KW - FACILE SYNTHESIS

KW - SALICYL ALCOHOL

U2 - 10.1002/anie.200462642

DO - 10.1002/anie.200462642

M3 - Journal article

VL - 44

SP - 1870

EP - 1873

JO - Angewandte Chemie International Edition

JF - Angewandte Chemie International Edition

SN - 1433-7851

IS - 12

ER -