Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry

Simple, straightforward and optimized procedures for preparing extended π-conjugated linkers are described. Either unsubstituted or 4-donor substituted π-linkers bearing a styryl, biphenyl, phenylethenylphenyl, and phenylethynylphenyl π-conjugated backbone are functionalized with boronic pinacol est...

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Main Authors: Jiří Kulhánek, Filip Bureš, Miroslav Ludwig
Format: Article
Language:English
Published: Beilstein-Institut 2009-04-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.5.11
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spelling doaj-6b6b1a17028744eea0f7815e8f97dcb62021-02-02T07:54:14ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972009-04-01511110.3762/bjoc.5.111860-5397-5-11Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistryJiří Kulhánek0Filip Bureš1Miroslav Ludwig2Institute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, nám Čs. legií 565, Pardubice, 532 10, Czech RepublicInstitute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, nám Čs. legií 565, Pardubice, 532 10, Czech RepublicInstitute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, nám Čs. legií 565, Pardubice, 532 10, Czech RepublicSimple, straightforward and optimized procedures for preparing extended π-conjugated linkers are described. Either unsubstituted or 4-donor substituted π-linkers bearing a styryl, biphenyl, phenylethenylphenyl, and phenylethynylphenyl π-conjugated backbone are functionalized with boronic pinacol esters as well as with terminal acetylene moieties allowing their further use as building blocks in Suzuki–Miyaura or Sonogashira coupling reactions.https://doi.org/10.3762/bjoc.5.11boronic aciddonor/acceptorlinkerSonogashira reactionproperty tuningpush-pullSuzuki–Miyaura reaction
collection DOAJ
language English
format Article
sources DOAJ
author Jiří Kulhánek
Filip Bureš
Miroslav Ludwig
spellingShingle Jiří Kulhánek
Filip Bureš
Miroslav Ludwig
Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry
Beilstein Journal of Organic Chemistry
boronic acid
donor/acceptor
linker
Sonogashira reaction
property tuning
push-pull
Suzuki–Miyaura reaction
author_facet Jiří Kulhánek
Filip Bureš
Miroslav Ludwig
author_sort Jiří Kulhánek
title Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry
title_short Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry
title_full Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry
title_fullStr Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry
title_full_unstemmed Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry
title_sort convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry
publisher Beilstein-Institut
series Beilstein Journal of Organic Chemistry
issn 1860-5397
publishDate 2009-04-01
description Simple, straightforward and optimized procedures for preparing extended π-conjugated linkers are described. Either unsubstituted or 4-donor substituted π-linkers bearing a styryl, biphenyl, phenylethenylphenyl, and phenylethynylphenyl π-conjugated backbone are functionalized with boronic pinacol esters as well as with terminal acetylene moieties allowing their further use as building blocks in Suzuki–Miyaura or Sonogashira coupling reactions.
topic boronic acid
donor/acceptor
linker
Sonogashira reaction
property tuning
push-pull
Suzuki–Miyaura reaction
url https://doi.org/10.3762/bjoc.5.11
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AT miroslavludwig convenientmethodsforpreparingpconjugatedlinkersasbuildingblocksformodularchemistry
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