Literature DB >> 11457142

New fluorogenic probes for oxygen and carbene transfer: a sensitive assay for single bead-supported catalysts.

M Havranek1, R Moreira, D Sames.   

Abstract

A high-throughput screening assay for atom transfer catalysis has been developed. This assay is based on two probes, developed herein, which generate highly fluorescent products upon carbene or oxygen atom transfer. The emission wavelength of probes 1 and 5 shift significantly (up to 90 nm) upon epoxidation, allowing detection of product at 3% conversion. Probe 7 is not fluorescent, while fluorescence emission by carbene insertion/rearrangement product 8 allows detection at less than 1% conversion. Such sensitivity allows for examination of single-bead reactions in a high throughput array format (1536 wells per plate), and provides a broad detection window ranging from single to high turnover numbers. Thousands of metal complexes are evaluated in a single screening experiment. Preliminary screening of a diverse ligand library with probe 7 in the presence of Rh(II) uncovered new catalysts capable of cyclopropanation and C-H insertion.

Entities:  

Year:  2001        PMID: 11457142     DOI: 10.1021/ja003786+

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


  5 in total

1.  In situ enzymatic screening (ISES): a tool for catalyst discovery and reaction development.

Authors:  David B Berkowitz; Mohua Bose; Sungjo Choi
Journal:  Angew Chem Int Ed Engl       Date:  2002-05-03       Impact factor: 15.336

Review 2.  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

3.  One-bead-one-catalyst approach to aspartic acid-based oxidation catalyst discovery.

Authors:  Phillip A Lichtor; Scott J Miller
Journal:  ACS Comb Sci       Date:  2011-04-06       Impact factor: 3.784

4.  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

5.  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

  5 in total

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