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Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes

Safe- and convenient-to-handle surrogates of hazardous chemicals are always in demand. Recently introduced cyclohexa-1,4-dienes with adequate substitution fulfil this role as El(+)/H(–) equivalents in B(C(6)F(5))(3)-catalysed transfer reactions of El–H to π- and σ-donors (C[double bond, length as m-...

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Detalles Bibliográficos
Autores principales: Keess, Sebastian, Oestreich, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596415/
https://www.ncbi.nlm.nih.gov/pubmed/28936336
http://dx.doi.org/10.1039/c7sc01657c
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author Keess, Sebastian
Oestreich, Martin
author_facet Keess, Sebastian
Oestreich, Martin
author_sort Keess, Sebastian
collection PubMed
description Safe- and convenient-to-handle surrogates of hazardous chemicals are always in demand. Recently introduced cyclohexa-1,4-dienes with adequate substitution fulfil this role as El(+)/H(–) equivalents in B(C(6)F(5))(3)-catalysed transfer reactions of El–H to π- and σ-donors (C[double bond, length as m-dash]C/C[triple bond, length as m-dash]C and C[double bond, length as m-dash]O/C[double bond, length as m-dash]N). Surrogates of Si–H/Ge–H, H–H and even C–H bonds have been designed and successfully applied to ionic transfer hydrosilylation/hydrogermylation, hydrogenation and hydro-tert-butylation, respectively. These processes and their basic principles are summarised in this Minireview. The similarities and differences between these transfer reactions as well as the challenges associated with these transformations are discussed.
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spelling pubmed-55964152017-09-21 Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes Keess, Sebastian Oestreich, Martin Chem Sci Chemistry Safe- and convenient-to-handle surrogates of hazardous chemicals are always in demand. Recently introduced cyclohexa-1,4-dienes with adequate substitution fulfil this role as El(+)/H(–) equivalents in B(C(6)F(5))(3)-catalysed transfer reactions of El–H to π- and σ-donors (C[double bond, length as m-dash]C/C[triple bond, length as m-dash]C and C[double bond, length as m-dash]O/C[double bond, length as m-dash]N). Surrogates of Si–H/Ge–H, H–H and even C–H bonds have been designed and successfully applied to ionic transfer hydrosilylation/hydrogermylation, hydrogenation and hydro-tert-butylation, respectively. These processes and their basic principles are summarised in this Minireview. The similarities and differences between these transfer reactions as well as the challenges associated with these transformations are discussed. Royal Society of Chemistry 2017-07-01 2017-05-24 /pmc/articles/PMC5596415/ /pubmed/28936336 http://dx.doi.org/10.1039/c7sc01657c Text en This journal is © The Royal Society of Chemistry 2017 https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Keess, Sebastian
Oestreich, Martin
Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes
title Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes
title_full Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes
title_fullStr Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes
title_full_unstemmed Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes
title_short Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes
title_sort cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596415/
https://www.ncbi.nlm.nih.gov/pubmed/28936336
http://dx.doi.org/10.1039/c7sc01657c
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