Synthesis of biaryl-styrene monomers by microwave-assisted Suzuki coupling

Hazit A. Zayas; Michael C. Bowyer; Christopher P. Gordon; Clovia I. Holdsworth; Adam McCluskey

doi:10.1016/j.tetlet.2009.07.117

Synthesis of biaryl-styrene monomers by microwave-assisted Suzuki coupling

Hazit A. Zayas, Michael C. Bowyer, Christopher P. Gordon, Clovia I. Holdsworth, Adam McCluskey

Research output: Contribution to journal › Article › peer-review

12 Citations (Scopus)

Abstract

Biaryl-styrenic monomers are prepared via Suzuki coupling as functional monomers in the synthesis of molecularly imprinted polymers. Traditional thermal Suzuki approaches are hampered by competition between Suzuki, Heck and homo-coupling reactions. Microwave-assisted approaches facilitated rapid access to the desired Suzuki products whilst suppressing both Heck and homo-couplings of 4-vinylboronic acid.

Original language	English
Pages (from-to)	5894-5895
Number of pages	2
Journal	Tetrahedron Letters
Volume	50
Issue number	43
DOIs	https://doi.org/10.1016/j.tetlet.2009.07.117
Publication status	Published - 2009

Access to Document

10.1016/j.tetlet.2009.07.117

Cite this

@article{4c35569451cf4aada7b23277fd4c5d36,

title = "Synthesis of biaryl-styrene monomers by microwave-assisted Suzuki coupling",

abstract = "Biaryl-styrenic monomers are prepared via Suzuki coupling as functional monomers in the synthesis of molecularly imprinted polymers. Traditional thermal Suzuki approaches are hampered by competition between Suzuki, Heck and homo-coupling reactions. Microwave-assisted approaches facilitated rapid access to the desired Suzuki products whilst suppressing both Heck and homo-couplings of 4-vinylboronic acid.",

author = "Zayas, {Hazit A.} and Bowyer, {Michael C.} and Gordon, {Christopher P.} and Holdsworth, {Clovia I.} and Adam McCluskey",

year = "2009",

doi = "10.1016/j.tetlet.2009.07.117",

language = "English",

volume = "50",

pages = "5894--5895",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "43",

}

TY - JOUR

T1 - Synthesis of biaryl-styrene monomers by microwave-assisted Suzuki coupling

AU - Zayas, Hazit A.

AU - Bowyer, Michael C.

AU - Gordon, Christopher P.

AU - Holdsworth, Clovia I.

AU - McCluskey, Adam

PY - 2009

Y1 - 2009

N2 - Biaryl-styrenic monomers are prepared via Suzuki coupling as functional monomers in the synthesis of molecularly imprinted polymers. Traditional thermal Suzuki approaches are hampered by competition between Suzuki, Heck and homo-coupling reactions. Microwave-assisted approaches facilitated rapid access to the desired Suzuki products whilst suppressing both Heck and homo-couplings of 4-vinylboronic acid.

AB - Biaryl-styrenic monomers are prepared via Suzuki coupling as functional monomers in the synthesis of molecularly imprinted polymers. Traditional thermal Suzuki approaches are hampered by competition between Suzuki, Heck and homo-coupling reactions. Microwave-assisted approaches facilitated rapid access to the desired Suzuki products whilst suppressing both Heck and homo-couplings of 4-vinylboronic acid.

UR - http://handle.uws.edu.au:8081/1959.7/546916

U2 - 10.1016/j.tetlet.2009.07.117

DO - 10.1016/j.tetlet.2009.07.117

M3 - Article

SN - 0040-4039

VL - 50

SP - 5894

EP - 5895

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 43

ER -

Synthesis of biaryl-styrene monomers by microwave-assisted Suzuki coupling

Abstract

Access to Document

Other files and links

Fingerprint

Cite this