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An alkyne hydrosilylation-Hiyama coupling approach to highly functionalised 1,3-dienes

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

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An alkyne hydrosilylation-Hiyama coupling approach to highly functionalised 1,3-dienes. / McAdam, C.A.; McLaughlin, M.G.; Cook, M.J.
In: Organic Chemistry Frontiers, Vol. 2, No. 5, 01.05.2015, p. 510-514.

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

Harvard

McAdam, CA, McLaughlin, MG & Cook, MJ 2015, 'An alkyne hydrosilylation-Hiyama coupling approach to highly functionalised 1,3-dienes', Organic Chemistry Frontiers, vol. 2, no. 5, pp. 510-514. https://doi.org/10.1039/c5qo00002e

APA

McAdam, C. A., McLaughlin, M. G., & Cook, M. J. (2015). An alkyne hydrosilylation-Hiyama coupling approach to highly functionalised 1,3-dienes. Organic Chemistry Frontiers, 2(5), 510-514. https://doi.org/10.1039/c5qo00002e

Vancouver

McAdam CA, McLaughlin MG, Cook MJ. An alkyne hydrosilylation-Hiyama coupling approach to highly functionalised 1,3-dienes. Organic Chemistry Frontiers. 2015 May 1;2(5):510-514. Epub 2015 Mar 17. doi: 10.1039/c5qo00002e

Author

McAdam, C.A. ; McLaughlin, M.G. ; Cook, M.J. / An alkyne hydrosilylation-Hiyama coupling approach to highly functionalised 1,3-dienes. In: Organic Chemistry Frontiers. 2015 ; Vol. 2, No. 5. pp. 510-514.

Bibtex

@article{71fea9fde2a54c9fae0ca0420a674643,
title = "An alkyne hydrosilylation-Hiyama coupling approach to highly functionalised 1,3-dienes",
abstract = "A high yielding and robust protocol for the stereodefined synthesis of 1,3-dienes has been established through a hydrosilylation–Hiyama coupling strategy. In all cases the products were formed as single E,E isomers and conditions are tolerant of a wide range of functional groups not compatible with other methods.",
author = "C.A. McAdam and M.G. McLaughlin and M.J. Cook",
year = "2015",
month = may,
day = "1",
doi = "10.1039/c5qo00002e",
language = "English",
volume = "2",
pages = "510--514",
journal = "Organic Chemistry Frontiers",
publisher = "Royal Society of Chemistry",
number = "5",

}

RIS

TY - JOUR

T1 - An alkyne hydrosilylation-Hiyama coupling approach to highly functionalised 1,3-dienes

AU - McAdam, C.A.

AU - McLaughlin, M.G.

AU - Cook, M.J.

PY - 2015/5/1

Y1 - 2015/5/1

N2 - A high yielding and robust protocol for the stereodefined synthesis of 1,3-dienes has been established through a hydrosilylation–Hiyama coupling strategy. In all cases the products were formed as single E,E isomers and conditions are tolerant of a wide range of functional groups not compatible with other methods.

AB - A high yielding and robust protocol for the stereodefined synthesis of 1,3-dienes has been established through a hydrosilylation–Hiyama coupling strategy. In all cases the products were formed as single E,E isomers and conditions are tolerant of a wide range of functional groups not compatible with other methods.

U2 - 10.1039/c5qo00002e

DO - 10.1039/c5qo00002e

M3 - Journal article

VL - 2

SP - 510

EP - 514

JO - Organic Chemistry Frontiers

JF - Organic Chemistry Frontiers

IS - 5

ER -