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One-pot multistep mechanochemical synthesis of fluorinated pyrazolones

Solventless mechanochemical synthesis represents a technique with improved sustainability metrics compared to solvent-based processes. Herein, we describe a methodical process to run one solventless reaction directly into another through multistep mechanochemistry, effectively amplifying the solvent...

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Autores principales: Howard, Joseph L, Nicholson, William, Sagatov, Yerbol, Browne, Duncan L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629391/
https://www.ncbi.nlm.nih.gov/pubmed/29062413
http://dx.doi.org/10.3762/bjoc.13.189
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author Howard, Joseph L
Nicholson, William
Sagatov, Yerbol
Browne, Duncan L
author_facet Howard, Joseph L
Nicholson, William
Sagatov, Yerbol
Browne, Duncan L
author_sort Howard, Joseph L
collection PubMed
description Solventless mechanochemical synthesis represents a technique with improved sustainability metrics compared to solvent-based processes. Herein, we describe a methodical process to run one solventless reaction directly into another through multistep mechanochemistry, effectively amplifying the solvent savings. The approach has to consider the solid form of the materials and compatibility of any auxiliary used. This has culminated in the development of a two-step, one-jar protocol for heterocycle formation and subsequent fluorination that has been successfully applied across a range of substrates, resulting in 12 difluorinated pyrazolones in moderate to excellent yields.
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spelling pubmed-56293912017-10-23 One-pot multistep mechanochemical synthesis of fluorinated pyrazolones Howard, Joseph L Nicholson, William Sagatov, Yerbol Browne, Duncan L Beilstein J Org Chem Full Research Paper Solventless mechanochemical synthesis represents a technique with improved sustainability metrics compared to solvent-based processes. Herein, we describe a methodical process to run one solventless reaction directly into another through multistep mechanochemistry, effectively amplifying the solvent savings. The approach has to consider the solid form of the materials and compatibility of any auxiliary used. This has culminated in the development of a two-step, one-jar protocol for heterocycle formation and subsequent fluorination that has been successfully applied across a range of substrates, resulting in 12 difluorinated pyrazolones in moderate to excellent yields. Beilstein-Institut 2017-09-14 /pmc/articles/PMC5629391/ /pubmed/29062413 http://dx.doi.org/10.3762/bjoc.13.189 Text en Copyright © 2017, Howard 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 Full Research Paper
Howard, Joseph L
Nicholson, William
Sagatov, Yerbol
Browne, Duncan L
One-pot multistep mechanochemical synthesis of fluorinated pyrazolones
title One-pot multistep mechanochemical synthesis of fluorinated pyrazolones
title_full One-pot multistep mechanochemical synthesis of fluorinated pyrazolones
title_fullStr One-pot multistep mechanochemical synthesis of fluorinated pyrazolones
title_full_unstemmed One-pot multistep mechanochemical synthesis of fluorinated pyrazolones
title_short One-pot multistep mechanochemical synthesis of fluorinated pyrazolones
title_sort one-pot multistep mechanochemical synthesis of fluorinated pyrazolones
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629391/
https://www.ncbi.nlm.nih.gov/pubmed/29062413
http://dx.doi.org/10.3762/bjoc.13.189
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