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...
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Online Access: | https://doi.org/10.3762/bjoc.13.220 |
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doaj-7de863303bc5433fa7c5f1e3fe2c09e62021-02-02T08:19:11ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972017-10-011312214223410.3762/bjoc.13.2201860-5397-13-220Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspectiveYaroslav D. Boyko0Valentin S. Dorokhov1Alexey Yu. Sukhorukov2Sema L. Ioffe3N. D. Zelinsky Institute of Organic Chemistry, 119991, Leninsky prospect, 47, Moscow, RussiaN. D. Zelinsky Institute of Organic Chemistry, 119991, Leninsky prospect, 47, Moscow, RussiaN. D. Zelinsky Institute of Organic Chemistry, 119991, Leninsky prospect, 47, Moscow, RussiaN. D. Zelinsky Institute of Organic Chemistry, 119991, Leninsky prospect, 47, Moscow, RussiaDespite 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.https://doi.org/10.3762/bjoc.13.220carbon–carbon bond formationMichael additionnitrosoalkenesoximestotal synthesis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yaroslav D. Boyko Valentin S. Dorokhov Alexey Yu. Sukhorukov Sema L. Ioffe |
spellingShingle |
Yaroslav D. Boyko Valentin S. Dorokhov Alexey Yu. Sukhorukov Sema L. Ioffe Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective Beilstein Journal of Organic Chemistry carbon–carbon bond formation Michael addition nitrosoalkenes oximes total synthesis |
author_facet |
Yaroslav D. Boyko Valentin S. Dorokhov Alexey Yu. Sukhorukov Sema L. Ioffe |
author_sort |
Yaroslav D. Boyko |
title |
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_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_sort |
conjugated nitrosoalkenes as michael acceptors in carbon–carbon bond forming reactions: a review and perspective |
publisher |
Beilstein-Institut |
series |
Beilstein Journal of Organic Chemistry |
issn |
1860-5397 |
publishDate |
2017-10-01 |
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. |
topic |
carbon–carbon bond formation Michael addition nitrosoalkenes oximes total synthesis |
url |
https://doi.org/10.3762/bjoc.13.220 |
work_keys_str_mv |
AT yaroslavdboyko conjugatednitrosoalkenesasmichaelacceptorsincarboncarbonbondformingreactionsareviewandperspective AT valentinsdorokhov conjugatednitrosoalkenesasmichaelacceptorsincarboncarbonbondformingreactionsareviewandperspective AT alexeyyusukhorukov conjugatednitrosoalkenesasmichaelacceptorsincarboncarbonbondformingreactionsareviewandperspective AT semalioffe conjugatednitrosoalkenesasmichaelacceptorsincarboncarbonbondformingreactionsareviewandperspective |
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1724297374304567296 |