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Allylic alcohol synthesis by Ni-catalyzed direct and selective coupling of alkynes and methanol
Methanol is an abundant and renewable chemical raw material, but its use as a C1 source in C–C bond coupling reactions still constitutes a big challenge, and the known methods are limited to the use of expensive and noble metal catalysts such as Ru, Rh and Ir. We herein report nickel-catalyzed direc...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278963/ https://www.ncbi.nlm.nih.gov/pubmed/34349909 http://dx.doi.org/10.1039/d1sc02625a |
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author | Chen, Herong Zhou, Zhijun Kong, Wangqing |
author_facet | Chen, Herong Zhou, Zhijun Kong, Wangqing |
author_sort | Chen, Herong |
collection | PubMed |
description | Methanol is an abundant and renewable chemical raw material, but its use as a C1 source in C–C bond coupling reactions still constitutes a big challenge, and the known methods are limited to the use of expensive and noble metal catalysts such as Ru, Rh and Ir. We herein report nickel-catalyzed direct coupling of alkynes and methanol, providing direct access to valuable allylic alcohols in good yields and excellent chemo- and regioselectivity. The approach features a broad substrate scope and high atom-, step- and redox-economy. Moreover, this method was successfully extended to the synthesis of [5,6]-bicyclic hemiacetals through a cascade cyclization reaction of alkynones and methanol. |
format | Online Article Text |
id | pubmed-8278963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-82789632021-08-03 Allylic alcohol synthesis by Ni-catalyzed direct and selective coupling of alkynes and methanol Chen, Herong Zhou, Zhijun Kong, Wangqing Chem Sci Chemistry Methanol is an abundant and renewable chemical raw material, but its use as a C1 source in C–C bond coupling reactions still constitutes a big challenge, and the known methods are limited to the use of expensive and noble metal catalysts such as Ru, Rh and Ir. We herein report nickel-catalyzed direct coupling of alkynes and methanol, providing direct access to valuable allylic alcohols in good yields and excellent chemo- and regioselectivity. The approach features a broad substrate scope and high atom-, step- and redox-economy. Moreover, this method was successfully extended to the synthesis of [5,6]-bicyclic hemiacetals through a cascade cyclization reaction of alkynones and methanol. The Royal Society of Chemistry 2021-06-07 /pmc/articles/PMC8278963/ /pubmed/34349909 http://dx.doi.org/10.1039/d1sc02625a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Chen, Herong Zhou, Zhijun Kong, Wangqing Allylic alcohol synthesis by Ni-catalyzed direct and selective coupling of alkynes and methanol |
title | Allylic alcohol synthesis by Ni-catalyzed direct and selective coupling of alkynes and methanol |
title_full | Allylic alcohol synthesis by Ni-catalyzed direct and selective coupling of alkynes and methanol |
title_fullStr | Allylic alcohol synthesis by Ni-catalyzed direct and selective coupling of alkynes and methanol |
title_full_unstemmed | Allylic alcohol synthesis by Ni-catalyzed direct and selective coupling of alkynes and methanol |
title_short | Allylic alcohol synthesis by Ni-catalyzed direct and selective coupling of alkynes and methanol |
title_sort | allylic alcohol synthesis by ni-catalyzed direct and selective coupling of alkynes and methanol |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278963/ https://www.ncbi.nlm.nih.gov/pubmed/34349909 http://dx.doi.org/10.1039/d1sc02625a |
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