Fluorescent Detection of Carbon−Carbon Bond Formation
- 21 June 2003
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 125 (28) , 8523-8528
- https://doi.org/10.1021/ja034069t
Abstract
We have developed a new spectroscopic system for detecting carbon−carbon bond formation by fluorescence to enhance high-throughput catalyst screening and rapid characterization of catalysts on a small scale. Fluorogenic substrates composed of a fluorophore possessing an amino group are readily prepared as amides of α,β-unsaturated carbonyl compounds and generally exhibit low fluorescence, while Michael or Diels−Alder reactions of these fluorogenic substrates provide products of significantly increased fluorescence. The product's fluorescence is approximately 20- to 100-fold higher than that of the substrate. The assay system was validated by screening potential catalysts of the Michael reaction and in solvent optimization experiments. The covalent combination of fluorophores possessing an amino group with α,β-unsaturated carbonyl compounds should provide a diverse range of fluorogenic substrates that may be used to rapidly screen catalysts and to optimize reaction conditions.Keywords
This publication has 22 references indexed in Scilit:
- Phage display selection of peptides possessing aldolase activityChemical Communications, 2001
- Reconstructing Aldolase Antibodies to Alter Their Substrate Specificity and TurnoverJournal of the American Chemical Society, 2000
- A Fluorescence-Based Assay for High-Throughput Screening of Coupling Reactions. Application to Heck ChemistryJournal of the American Chemical Society, 1999
- Combinatorial and rapid screening approaches to homogeneous catalyst discovery and optimizationChemical Communications, 1999
- Reactive Dyes as a Method for Rapid Screening of Homogeneous CatalystsJournal of the American Chemical Society, 1998
- Aldolase Antibodies of Remarkable ScopeJournal of the American Chemical Society, 1998
- Immune Versus Natural Selection: Antibody Aldolases with Enzymic Rates But Broader ScopeScience, 1997
- Asymmetric Michael Addition of Malonate Anions to Prochiral Acceptors Catalyzed by l-Proline Rubidium SaltThe Journal of Organic Chemistry, 1996
- Efficient Aldolase Catalytic Antibodies That Use the Enamine Mechanism of Natural EnzymesScience, 1995
- Analogs of .gamma.-hydroxybutyric acid. Synthesis and binding studiesJournal of Medicinal Chemistry, 1988