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Small Molecule Library Synthesis Using Segmented Flow

Flow chemistry has gained considerable recognition as a simple, efficient, and safe technology for the synthesis of many types of organic and inorganic molecules ranging in scope from large complex natural products to silicon nanoparticles. In this paper we describe a method that adapts flow chemist...

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Autores principales: Thompson, Christina M., Poole, Jennifer L., Cross, Jeffrey L., Akritopoulou-Zanze, Irini, Djuric, Stevan W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264587/
https://www.ncbi.nlm.nih.gov/pubmed/22048699
http://dx.doi.org/10.3390/molecules16119161
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author Thompson, Christina M.
Poole, Jennifer L.
Cross, Jeffrey L.
Akritopoulou-Zanze, Irini
Djuric, Stevan W.
author_facet Thompson, Christina M.
Poole, Jennifer L.
Cross, Jeffrey L.
Akritopoulou-Zanze, Irini
Djuric, Stevan W.
author_sort Thompson, Christina M.
collection PubMed
description Flow chemistry has gained considerable recognition as a simple, efficient, and safe technology for the synthesis of many types of organic and inorganic molecules ranging in scope from large complex natural products to silicon nanoparticles. In this paper we describe a method that adapts flow chemistry to the synthesis of libraries of compounds using a fluorous immiscible solvent as a spacer between reactions. The methodology was validated in the synthesis of two small heterocycle containing libraries. The reactions were performed on a 0.2 mmol scale, enabling tens of milligrams of material to be generated in a single 200 μL reaction plug. The methodology allowed library synthesis in half the time of conventional microwave synthesis while maintaining similar yields. The ability to perform multiple, potentially unrelated reactions in a single run is ideal for making small quantities of many different compounds quickly and efficiently.
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spelling pubmed-62645872018-12-10 Small Molecule Library Synthesis Using Segmented Flow Thompson, Christina M. Poole, Jennifer L. Cross, Jeffrey L. Akritopoulou-Zanze, Irini Djuric, Stevan W. Molecules Article Flow chemistry has gained considerable recognition as a simple, efficient, and safe technology for the synthesis of many types of organic and inorganic molecules ranging in scope from large complex natural products to silicon nanoparticles. In this paper we describe a method that adapts flow chemistry to the synthesis of libraries of compounds using a fluorous immiscible solvent as a spacer between reactions. The methodology was validated in the synthesis of two small heterocycle containing libraries. The reactions were performed on a 0.2 mmol scale, enabling tens of milligrams of material to be generated in a single 200 μL reaction plug. The methodology allowed library synthesis in half the time of conventional microwave synthesis while maintaining similar yields. The ability to perform multiple, potentially unrelated reactions in a single run is ideal for making small quantities of many different compounds quickly and efficiently. MDPI 2011-11-02 /pmc/articles/PMC6264587/ /pubmed/22048699 http://dx.doi.org/10.3390/molecules16119161 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Thompson, Christina M.
Poole, Jennifer L.
Cross, Jeffrey L.
Akritopoulou-Zanze, Irini
Djuric, Stevan W.
Small Molecule Library Synthesis Using Segmented Flow
title Small Molecule Library Synthesis Using Segmented Flow
title_full Small Molecule Library Synthesis Using Segmented Flow
title_fullStr Small Molecule Library Synthesis Using Segmented Flow
title_full_unstemmed Small Molecule Library Synthesis Using Segmented Flow
title_short Small Molecule Library Synthesis Using Segmented Flow
title_sort small molecule library synthesis using segmented flow
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264587/
https://www.ncbi.nlm.nih.gov/pubmed/22048699
http://dx.doi.org/10.3390/molecules16119161
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