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Three-Component Reaction Discovery Enabled by Mass Spectrometry of Self-Assembled Monolayers

Multi-component reactions have been extensively employed in many areas of organic chemistry. Despite significant progress, the discovery of such enabling transformations remains challenging. Here, we present the development of a parallel, label-free reaction-discovery platform, which can be used for...

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Autores principales: Montavon, Timothy J., Li, Jing, Cabrera-Pardo, Jaime R., Mrksich, Milan, Kozmin, Sergey A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3243075/
https://www.ncbi.nlm.nih.gov/pubmed/22169871
http://dx.doi.org/10.1038/nchem.1212
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author Montavon, Timothy J.
Li, Jing
Cabrera-Pardo, Jaime R.
Mrksich, Milan
Kozmin, Sergey A.
author_facet Montavon, Timothy J.
Li, Jing
Cabrera-Pardo, Jaime R.
Mrksich, Milan
Kozmin, Sergey A.
author_sort Montavon, Timothy J.
collection PubMed
description Multi-component reactions have been extensively employed in many areas of organic chemistry. Despite significant progress, the discovery of such enabling transformations remains challenging. Here, we present the development of a parallel, label-free reaction-discovery platform, which can be used for identification of new multi-component transformations. Our approach is based on the parallel mass spectrometric screening of interfacial chemical reactions on arrays of self-assembled monolayers. This strategy enabled the identification of a simple organic phosphine that can catalyze a previously unknown condensation of siloxy alkynes, aldehydes and amines to produce 3-hydroxy amides with high efficiency and diastereoselectivity. The reaction was further optimized using solution phase methods.
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spelling pubmed-32430752012-07-01 Three-Component Reaction Discovery Enabled by Mass Spectrometry of Self-Assembled Monolayers Montavon, Timothy J. Li, Jing Cabrera-Pardo, Jaime R. Mrksich, Milan Kozmin, Sergey A. Nat Chem Article Multi-component reactions have been extensively employed in many areas of organic chemistry. Despite significant progress, the discovery of such enabling transformations remains challenging. Here, we present the development of a parallel, label-free reaction-discovery platform, which can be used for identification of new multi-component transformations. Our approach is based on the parallel mass spectrometric screening of interfacial chemical reactions on arrays of self-assembled monolayers. This strategy enabled the identification of a simple organic phosphine that can catalyze a previously unknown condensation of siloxy alkynes, aldehydes and amines to produce 3-hydroxy amides with high efficiency and diastereoselectivity. The reaction was further optimized using solution phase methods. 2011-12-04 /pmc/articles/PMC3243075/ /pubmed/22169871 http://dx.doi.org/10.1038/nchem.1212 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Montavon, Timothy J.
Li, Jing
Cabrera-Pardo, Jaime R.
Mrksich, Milan
Kozmin, Sergey A.
Three-Component Reaction Discovery Enabled by Mass Spectrometry of Self-Assembled Monolayers
title Three-Component Reaction Discovery Enabled by Mass Spectrometry of Self-Assembled Monolayers
title_full Three-Component Reaction Discovery Enabled by Mass Spectrometry of Self-Assembled Monolayers
title_fullStr Three-Component Reaction Discovery Enabled by Mass Spectrometry of Self-Assembled Monolayers
title_full_unstemmed Three-Component Reaction Discovery Enabled by Mass Spectrometry of Self-Assembled Monolayers
title_short Three-Component Reaction Discovery Enabled by Mass Spectrometry of Self-Assembled Monolayers
title_sort three-component reaction discovery enabled by mass spectrometry of self-assembled monolayers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3243075/
https://www.ncbi.nlm.nih.gov/pubmed/22169871
http://dx.doi.org/10.1038/nchem.1212
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