Cargando…
[3 + 2]-Cycloaddition reaction of sydnones with alkynes
This review covers all known examples of [3 + 2]-cycloaddition between sydnones and both terminal as well as internal alkynes/cycloalkynes taken from literature since its discovery by Huisgen in 1962 up to the current date. Except enumeration of synthetic applications it also covers mechanistic stud...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009199/ https://www.ncbi.nlm.nih.gov/pubmed/29977399 http://dx.doi.org/10.3762/bjoc.14.113 |
_version_ | 1783333329586618368 |
---|---|
author | Hladíková, Veronika Váňa, Jiří Hanusek, Jiří |
author_facet | Hladíková, Veronika Váňa, Jiří Hanusek, Jiří |
author_sort | Hladíková, Veronika |
collection | PubMed |
description | This review covers all known examples of [3 + 2]-cycloaddition between sydnones and both terminal as well as internal alkynes/cycloalkynes taken from literature since its discovery by Huisgen in 1962 up to the current date. Except enumeration of synthetic applications it also covers mechanistic studies, catalysis, effects of substituents and reaction conditions influencing reaction rate and regioselectivity. |
format | Online Article Text |
id | pubmed-6009199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-60091992018-07-05 [3 + 2]-Cycloaddition reaction of sydnones with alkynes Hladíková, Veronika Váňa, Jiří Hanusek, Jiří Beilstein J Org Chem Review This review covers all known examples of [3 + 2]-cycloaddition between sydnones and both terminal as well as internal alkynes/cycloalkynes taken from literature since its discovery by Huisgen in 1962 up to the current date. Except enumeration of synthetic applications it also covers mechanistic studies, catalysis, effects of substituents and reaction conditions influencing reaction rate and regioselectivity. Beilstein-Institut 2018-06-05 /pmc/articles/PMC6009199/ /pubmed/29977399 http://dx.doi.org/10.3762/bjoc.14.113 Text en Copyright © 2018, Hladíková et al. https://creativecommons.org/licenses/by/4.0https://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/4.0), 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 | Review Hladíková, Veronika Váňa, Jiří Hanusek, Jiří [3 + 2]-Cycloaddition reaction of sydnones with alkynes |
title | [3 + 2]-Cycloaddition reaction of sydnones with alkynes |
title_full | [3 + 2]-Cycloaddition reaction of sydnones with alkynes |
title_fullStr | [3 + 2]-Cycloaddition reaction of sydnones with alkynes |
title_full_unstemmed | [3 + 2]-Cycloaddition reaction of sydnones with alkynes |
title_short | [3 + 2]-Cycloaddition reaction of sydnones with alkynes |
title_sort | [3 + 2]-cycloaddition reaction of sydnones with alkynes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009199/ https://www.ncbi.nlm.nih.gov/pubmed/29977399 http://dx.doi.org/10.3762/bjoc.14.113 |
work_keys_str_mv | AT hladikovaveronika 32cycloadditionreactionofsydnoneswithalkynes AT vanajiri 32cycloadditionreactionofsydnoneswithalkynes AT hanusekjiri 32cycloadditionreactionofsydnoneswithalkynes |