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Ammonium Ylide Mediated Cyclization Reactions

The use of readily accessible ammonium ylides for (asymmetric) transformations, especially cyclization reactions, has received considerable attention over the past two decades. A variety of highly enantioselective protocols to facilitate annulation reactions have recently been introduced as an alter...

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Detalles Bibliográficos
Autores principales: Roiser, Lukas, Zielke, Katharina, Waser, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130843/
https://www.ncbi.nlm.nih.gov/pubmed/30210965
http://dx.doi.org/10.1002/ajoc.201800091
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author Roiser, Lukas
Zielke, Katharina
Waser, Mario
author_facet Roiser, Lukas
Zielke, Katharina
Waser, Mario
author_sort Roiser, Lukas
collection PubMed
description The use of readily accessible ammonium ylides for (asymmetric) transformations, especially cyclization reactions, has received considerable attention over the past two decades. A variety of highly enantioselective protocols to facilitate annulation reactions have recently been introduced as an alternative to other common methods including S-ylide-mediated strategies. It is the intention of this short review to provide an introduction to this field by highlighting the potential of ammonium ylides for (asymmetric) cyclization reactions as well as to present the limitations and challenges of these methods.
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spelling pubmed-61308432018-09-10 Ammonium Ylide Mediated Cyclization Reactions Roiser, Lukas Zielke, Katharina Waser, Mario Asian J Org Chem Article The use of readily accessible ammonium ylides for (asymmetric) transformations, especially cyclization reactions, has received considerable attention over the past two decades. A variety of highly enantioselective protocols to facilitate annulation reactions have recently been introduced as an alternative to other common methods including S-ylide-mediated strategies. It is the intention of this short review to provide an introduction to this field by highlighting the potential of ammonium ylides for (asymmetric) cyclization reactions as well as to present the limitations and challenges of these methods. 2018-03-25 2018-05 /pmc/articles/PMC6130843/ /pubmed/30210965 http://dx.doi.org/10.1002/ajoc.201800091 Text en https://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Roiser, Lukas
Zielke, Katharina
Waser, Mario
Ammonium Ylide Mediated Cyclization Reactions
title Ammonium Ylide Mediated Cyclization Reactions
title_full Ammonium Ylide Mediated Cyclization Reactions
title_fullStr Ammonium Ylide Mediated Cyclization Reactions
title_full_unstemmed Ammonium Ylide Mediated Cyclization Reactions
title_short Ammonium Ylide Mediated Cyclization Reactions
title_sort ammonium ylide mediated cyclization reactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130843/
https://www.ncbi.nlm.nih.gov/pubmed/30210965
http://dx.doi.org/10.1002/ajoc.201800091
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