Literature DB >> 12783551

Fluorescence resonance energy transfer (FRET) as a high-throughput assay for coupling reactions. Arylation of amines as a case study.

Shaun R Stauffer1, John F Hartwig.   

Abstract

A solution-phase assay based on fluorescence resonance energy transfer (FRET) was developed for high-throughput screening of palladium catalyzed aminations of aryl halides. Dansylpiperazine was used as the fluorescent component and a chloro- or bromoarene tagged with an azodye as the quenching partner. Fluorescence intensities of reaction aliquots correlated linearly with reaction yield after dilution to appropriate concentrations. A library of 119 phosphine and heterocyclic carbene ligands was evaluated in duplicate reactions of two combinations. In general, the FRET assay displayed excellent reproducibility, with less than 5% of the duplicate experiments showing significant variability in yields. Among reactions producing greater than 50% yield, the average percent uncertainty was just 5%. For a small subset of sterically hindered ligands, differences in yields between 10 and 20% were observed between the substrates bearing dyes for the FRET assay and substrates that are unfunctionalized. However, the remaining catalyst combinations gave yields similar to those expected from literature precedent. In addition to an evaluation of the accuracy of the FRET assay, this work includes the use of the FRET assay to investigate relative activities of various catalysts for the amination of aryl bromides and chlorides and to find conditions for aminations in more polar solvents. Reactions with K(3)PO(4) base in aqueous mixtures of polar and nonpolar organic solvents were shown to be appropriate for the amination chemistry.

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Year:  2003        PMID: 12783551     DOI: 10.1021/ja034161p

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  10 in total

Review 1.  Contemporary screening approaches to reaction discovery and development.

Authors:  Karl D Collins; Tobias Gensch; Frank Glorius
Journal:  Nat Chem       Date:  2014-10       Impact factor: 24.427

2.  Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide.

Authors:  David S Surry; Stephen L Buchwald
Journal:  Chem Sci       Date:  2011       Impact factor: 9.825

3.  Combinatorial catalysis employing a visible enzymatic beacon in real time: synthetically versatile (pseudo)halometalation/carbocyclizations.

Authors:  Jacob A Friest; Sylvain Broussy; Woo Jin Chung; David B Berkowitz
Journal:  Angew Chem Int Ed Engl       Date:  2011-08-16       Impact factor: 15.336

4.  ESIPT-mediated photocycloadditions of 3-hydroxyquinolinones: development of a fluorescence quenching assay for reaction screening.

Authors:  Bing Xia; Baudouin Gerard; Danielle M Solano; Jiandi Wan; Guilford Jones; John A Porco
Journal:  Org Lett       Date:  2011-02-21       Impact factor: 6.005

5.  A fluorogenic aldehyde bearing a 1,2,3-triazole moiety for monitoring the progress of aldol reactions.

Authors:  Hai-Ming Guo; Fujie Tanaka
Journal:  J Org Chem       Date:  2009-03-20       Impact factor: 4.354

6.  Azide-Alkyne Click Conjugation on Quantum Dots by Selective Copper Coordination.

Authors:  Victor R Mann; Alexander S Powers; Drew C Tilley; Jon T Sack; Bruce E Cohen
Journal:  ACS Nano       Date:  2018-04-04       Impact factor: 15.881

7.  Optical monitoring of polymerizations in droplets with high temporal dynamic range.

Authors:  Andrew C Cavell; Veronica K Krasecki; Guoping Li; Abhishek Sharma; Hao Sun; Matthew P Thompson; Christopher J Forman; Si Yue Guo; Riley J Hickman; Katherine A Parrish; Alán Aspuru-Guzik; Leroy Cronin; Nathan C Gianneschi; Randall H Goldsmith
Journal:  Chem Sci       Date:  2020-02-04       Impact factor: 9.825

8.  Three-component reaction discovery enabled by mass spectrometry of self-assembled monolayers.

Authors:  Timothy J Montavon; Jing Li; Jaime R Cabrera-Pardo; Milan Mrksich; Sergey A Kozmin
Journal:  Nat Chem       Date:  2011-12-04       Impact factor: 24.427

9.  Lost in chemical space? Maps to support organometallic catalysis.

Authors:  Natalie Fey
Journal:  Chem Cent J       Date:  2015-06-18       Impact factor: 4.215

10.  Mini-ISES identifies promising carbafructopyranose-based salens for asymmetric catalysis: Tuning ligand shape via the anomeric effect.

Authors:  Kannan R Karukurichi; Xiang Fei; Robert A Swyka; Sylvain Broussy; Weijun Shen; Sangeeta Dey; Sandip K Roy; David B Berkowitz
Journal:  Sci Adv       Date:  2015-07-10       Impact factor: 14.136

  10 in total

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