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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...

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Detalles Bibliográficos
Autores principales: Chen, Herong, Zhou, Zhijun, Kong, Wangqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
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.
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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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AT kongwangqing allylicalcoholsynthesisbynicatalyzeddirectandselectivecouplingofalkynesandmethanol