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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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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. |
format | Online Article Text |
id | pubmed-6130843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT roiserlukas ammoniumylidemediatedcyclizationreactions AT zielkekatharina ammoniumylidemediatedcyclizationreactions AT wasermario ammoniumylidemediatedcyclizationreactions |