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MIDA–Vinylsilanes: Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes

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MIDA–Vinylsilanes: Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes. / McLaughlin, Mark; McAdam, C.A.; Cook, Matthew J. .
In: Organic Letters, Vol. 17, No. 1, 02.01.2015, p. 10-13.

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

Harvard

McLaughlin, M, McAdam, CA & Cook, MJ 2015, 'MIDA–Vinylsilanes: Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes', Organic Letters, vol. 17, no. 1, pp. 10-13. https://doi.org/10.1021/ol503065a

APA

McLaughlin, M., McAdam, C. A., & Cook, M. J. (2015). MIDA–Vinylsilanes: Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes. Organic Letters, 17(1), 10-13. https://doi.org/10.1021/ol503065a

Vancouver

McLaughlin M, McAdam CA, Cook MJ. MIDA–Vinylsilanes: Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes. Organic Letters. 2015 Jan 2;17(1):10-13. Epub 2014 Dec 16. doi: 10.1021/ol503065a

Author

McLaughlin, Mark ; McAdam, C.A. ; Cook, Matthew J. . / MIDA–Vinylsilanes : Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes. In: Organic Letters. 2015 ; Vol. 17, No. 1. pp. 10-13.

Bibtex

@article{960e09e882d74f728fd2997fdd3e6804,
title = "MIDA–Vinylsilanes: Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes",
abstract = "A rapid and stereodefined synthesis of MIDA–boryl vinylsilanes has been achieved through the hydrosilylation of an alkynylboronic ester. The E products which contain a silyl and boryl group can be selectively cross-coupled in a two-step bidirectional sequence to provide a rapid and high-yielding synthesis of complex styrenes.",
author = "Mark McLaughlin and C.A. McAdam and Cook, {Matthew J.}",
year = "2015",
month = jan,
day = "2",
doi = "10.1021/ol503065a",
language = "English",
volume = "17",
pages = "10--13",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "1",

}

RIS

TY - JOUR

T1 - MIDA–Vinylsilanes

T2 - Selective Cross-Couplings and Applications to the Synthesis of Functionalized Stilbenes

AU - McLaughlin, Mark

AU - McAdam, C.A.

AU - Cook, Matthew J.

PY - 2015/1/2

Y1 - 2015/1/2

N2 - A rapid and stereodefined synthesis of MIDA–boryl vinylsilanes has been achieved through the hydrosilylation of an alkynylboronic ester. The E products which contain a silyl and boryl group can be selectively cross-coupled in a two-step bidirectional sequence to provide a rapid and high-yielding synthesis of complex styrenes.

AB - A rapid and stereodefined synthesis of MIDA–boryl vinylsilanes has been achieved through the hydrosilylation of an alkynylboronic ester. The E products which contain a silyl and boryl group can be selectively cross-coupled in a two-step bidirectional sequence to provide a rapid and high-yielding synthesis of complex styrenes.

U2 - 10.1021/ol503065a

DO - 10.1021/ol503065a

M3 - Journal article

VL - 17

SP - 10

EP - 13

JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 1

ER -