A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design

Organic compounds that contain nitrogen are very important intermediates in pharmaceutical and chemical industry. Hydroamination is the reaction that can form C–N bond with high atom economy. The research progress in metals catalyzed hydroamination of alkenes and alkynes from the perspective of reac...

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Autores principales: Huo, Jingpei, He, Guozhang, Chen, Weilan, Hu, Xiaohong, Deng, Qianjun, Chen, Dongchu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661821/
https://www.ncbi.nlm.nih.gov/pubmed/31384836
http://dx.doi.org/10.1186/s13065-019-0606-7
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author Huo, Jingpei
He, Guozhang
Chen, Weilan
Hu, Xiaohong
Deng, Qianjun
Chen, Dongchu
author_facet Huo, Jingpei
He, Guozhang
Chen, Weilan
Hu, Xiaohong
Deng, Qianjun
Chen, Dongchu
author_sort Huo, Jingpei
collection PubMed
description Organic compounds that contain nitrogen are very important intermediates in pharmaceutical and chemical industry. Hydroamination is the reaction that can form C–N bond with high atom economy. The research progress in metals catalyzed hydroamination of alkenes and alkynes from the perspective of reaction mechanism is categorized and summarized. [Image: see text]
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spelling pubmed-66618212019-08-05 A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design Huo, Jingpei He, Guozhang Chen, Weilan Hu, Xiaohong Deng, Qianjun Chen, Dongchu BMC Chem Review Organic compounds that contain nitrogen are very important intermediates in pharmaceutical and chemical industry. Hydroamination is the reaction that can form C–N bond with high atom economy. The research progress in metals catalyzed hydroamination of alkenes and alkynes from the perspective of reaction mechanism is categorized and summarized. [Image: see text] Springer International Publishing 2019-07-11 /pmc/articles/PMC6661821/ /pubmed/31384836 http://dx.doi.org/10.1186/s13065-019-0606-7 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Huo, Jingpei
He, Guozhang
Chen, Weilan
Hu, Xiaohong
Deng, Qianjun
Chen, Dongchu
A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design
title A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design
title_full A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design
title_fullStr A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design
title_full_unstemmed A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design
title_short A minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design
title_sort minireview of hydroamination catalysis: alkene and alkyne substrate selective, metal complex design
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6661821/
https://www.ncbi.nlm.nih.gov/pubmed/31384836
http://dx.doi.org/10.1186/s13065-019-0606-7
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