Aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides

Metal catalyzed cross-coupling reactions have been the preferred tools to access to modified nucleosides (on the C5-position of pyrimidines and on the C7- or C8-positions of purines). Our objective is to focus this mini-review on the Suzuki-Miyaura and on the Heck cross-couplings of nucleosides usin...

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Autores principales: Hervé, Gwénaëlle, Len, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330919/
https://www.ncbi.nlm.nih.gov/pubmed/25741506
http://dx.doi.org/10.3389/fchem.2015.00010
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author Hervé, Gwénaëlle
Len, Christophe
author_facet Hervé, Gwénaëlle
Len, Christophe
author_sort Hervé, Gwénaëlle
collection PubMed
description Metal catalyzed cross-coupling reactions have been the preferred tools to access to modified nucleosides (on the C5-position of pyrimidines and on the C7- or C8-positions of purines). Our objective is to focus this mini-review on the Suzuki-Miyaura and on the Heck cross-couplings of nucleosides using microwave irradiations which is an alternative technology compatible with green chemistry and sustainable development
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spelling pubmed-43309192015-03-04 Aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides Hervé, Gwénaëlle Len, Christophe Front Chem Chemistry Metal catalyzed cross-coupling reactions have been the preferred tools to access to modified nucleosides (on the C5-position of pyrimidines and on the C7- or C8-positions of purines). Our objective is to focus this mini-review on the Suzuki-Miyaura and on the Heck cross-couplings of nucleosides using microwave irradiations which is an alternative technology compatible with green chemistry and sustainable development Frontiers Media S.A. 2015-02-17 /pmc/articles/PMC4330919/ /pubmed/25741506 http://dx.doi.org/10.3389/fchem.2015.00010 Text en Copyright © 2015 Hervé and Len. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Hervé, Gwénaëlle
Len, Christophe
Aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides
title Aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides
title_full Aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides
title_fullStr Aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides
title_full_unstemmed Aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides
title_short Aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides
title_sort aqueous microwave-assisted cross-coupling reactions applied to unprotected nucleosides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330919/
https://www.ncbi.nlm.nih.gov/pubmed/25741506
http://dx.doi.org/10.3389/fchem.2015.00010
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AT lenchristophe aqueousmicrowaveassistedcrosscouplingreactionsappliedtounprotectednucleosides

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