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Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective
Despite of their chemical instability and high reactivity, conjugated nitrosoalkenes are useful intermediates in target-oriented organic synthesis. The present review deals with carbon–carbon bond forming reactions involving Michael addition to α-nitrosoalkenes with a particular focus on recent deve...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Beilstein-Institut
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669230/ https://www.ncbi.nlm.nih.gov/pubmed/29114327 http://dx.doi.org/10.3762/bjoc.13.220 |
| _version_ | 1783275819249958912 |
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| author | Boyko, Yaroslav Dmitrievich Dorokhov, Valentin Sergeevich Sukhorukov, Alexey Yu Ioffe, Sema Leibovich |
| author_facet | Boyko, Yaroslav Dmitrievich Dorokhov, Valentin Sergeevich Sukhorukov, Alexey Yu Ioffe, Sema Leibovich |
| author_sort | Boyko, Yaroslav Dmitrievich |
| collection | PubMed |
| description | Despite of their chemical instability and high reactivity, conjugated nitrosoalkenes are useful intermediates in target-oriented organic synthesis. The present review deals with carbon–carbon bond forming reactions involving Michael addition to α-nitrosoalkenes with a particular focus on recent developments in this methodology and its use in total synthesis. |
| format | Online Article Text |
| id | pubmed-5669230 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2017 |
| publisher | Beilstein-Institut |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-56692302017-11-07 Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective Boyko, Yaroslav Dmitrievich Dorokhov, Valentin Sergeevich Sukhorukov, Alexey Yu Ioffe, Sema Leibovich Beilstein J Org Chem Review Despite of their chemical instability and high reactivity, conjugated nitrosoalkenes are useful intermediates in target-oriented organic synthesis. The present review deals with carbon–carbon bond forming reactions involving Michael addition to α-nitrosoalkenes with a particular focus on recent developments in this methodology and its use in total synthesis. Beilstein-Institut 2017-10-23 /pmc/articles/PMC5669230/ /pubmed/29114327 http://dx.doi.org/10.3762/bjoc.13.220 Text en Copyright © 2017, Boyko 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 Boyko, Yaroslav Dmitrievich Dorokhov, Valentin Sergeevich Sukhorukov, Alexey Yu Ioffe, Sema Leibovich Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective |
| title | Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective |
| title_full | Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective |
| title_fullStr | Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective |
| title_full_unstemmed | Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective |
| title_short | Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective |
| title_sort | conjugated nitrosoalkenes as michael acceptors in carbon–carbon bond forming reactions: a review and perspective |
| topic | Review |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669230/ https://www.ncbi.nlm.nih.gov/pubmed/29114327 http://dx.doi.org/10.3762/bjoc.13.220 |
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