Cargando…

The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow

The application of a monolithic form of triphenylphosphine to the Ramirez gem-dibromoolefination reaction using flow chemistry techniques is reported. A variety of gem-dibromides were synthesised in high purity and excellent yield following only removal of solvent and no further off-line purificatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Roper, Kimberley A, Berry, Malcolm B, Ley, Steven V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778394/
https://www.ncbi.nlm.nih.gov/pubmed/24062843
http://dx.doi.org/10.3762/bjoc.9.207
_version_ 1782285106040274944
author Roper, Kimberley A
Berry, Malcolm B
Ley, Steven V
author_facet Roper, Kimberley A
Berry, Malcolm B
Ley, Steven V
author_sort Roper, Kimberley A
collection PubMed
description The application of a monolithic form of triphenylphosphine to the Ramirez gem-dibromoolefination reaction using flow chemistry techniques is reported. A variety of gem-dibromides were synthesised in high purity and excellent yield following only removal of solvent and no further off-line purification. It is also possible to perform the Appel reaction using the same monolith and the relationship between the mechanisms of the two reactions is discussed.
format Online
Article
Text
id pubmed-3778394
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-37783942013-09-23 The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow Roper, Kimberley A Berry, Malcolm B Ley, Steven V Beilstein J Org Chem Full Research Paper The application of a monolithic form of triphenylphosphine to the Ramirez gem-dibromoolefination reaction using flow chemistry techniques is reported. A variety of gem-dibromides were synthesised in high purity and excellent yield following only removal of solvent and no further off-line purification. It is also possible to perform the Appel reaction using the same monolith and the relationship between the mechanisms of the two reactions is discussed. Beilstein-Institut 2013-09-02 /pmc/articles/PMC3778394/ /pubmed/24062843 http://dx.doi.org/10.3762/bjoc.9.207 Text en Copyright © 2013, Roper et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Roper, Kimberley A
Berry, Malcolm B
Ley, Steven V
The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow
title The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow
title_full The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow
title_fullStr The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow
title_full_unstemmed The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow
title_short The application of a monolithic triphenylphosphine reagent for conducting Ramirez gem-dibromoolefination reactions in flow
title_sort application of a monolithic triphenylphosphine reagent for conducting ramirez gem-dibromoolefination reactions in flow
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778394/
https://www.ncbi.nlm.nih.gov/pubmed/24062843
http://dx.doi.org/10.3762/bjoc.9.207
work_keys_str_mv AT roperkimberleya theapplicationofamonolithictriphenylphosphinereagentforconductingramirezgemdibromoolefinationreactionsinflow
AT berrymalcolmb theapplicationofamonolithictriphenylphosphinereagentforconductingramirezgemdibromoolefinationreactionsinflow
AT leystevenv theapplicationofamonolithictriphenylphosphinereagentforconductingramirezgemdibromoolefinationreactionsinflow
AT roperkimberleya applicationofamonolithictriphenylphosphinereagentforconductingramirezgemdibromoolefinationreactionsinflow
AT berrymalcolmb applicationofamonolithictriphenylphosphinereagentforconductingramirezgemdibromoolefinationreactionsinflow
AT leystevenv applicationofamonolithictriphenylphosphinereagentforconductingramirezgemdibromoolefinationreactionsinflow