Publikation: Mimicking Dimethylallyltryptophan Synthase : Experimental Evidence for a Biosynthetic Cope Rearrangement Process
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2012
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Angewandte Chemie International Edition. 2012, 51(46), pp. 11514-11516. ISSN 1433-7851. eISSN 1521-3773. Available under: doi: 10.1002/anie.201203586
Zusammenfassung
Experimental evidence was found to support an enzymatic [3,3]-sigmatropic rearrangement catalyzed by dimethylallyltryptophan (DMAT) synthase (see scheme). A bio-inspired system showed the feasibility of Cope rearrangement to the C-4 position of the indole nucleus. The tricyclic benzo[cd]indole core of welwitindolinones and dragmacidin E was synthesized using this transformation.
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SCHWARZER, Darius Daniel, Philipp J. GRITSCH, Tanja GAICH, 2012. Mimicking Dimethylallyltryptophan Synthase : Experimental Evidence for a Biosynthetic Cope Rearrangement Process. In: Angewandte Chemie International Edition. 2012, 51(46), pp. 11514-11516. ISSN 1433-7851. eISSN 1521-3773. Available under: doi: 10.1002/anie.201203586BibTex
@article{Schwarzer2012-11-12Mimic-38095,
year={2012},
doi={10.1002/anie.201203586},
title={Mimicking Dimethylallyltryptophan Synthase : Experimental Evidence for a Biosynthetic Cope Rearrangement Process},
number={46},
volume={51},
issn={1433-7851},
journal={Angewandte Chemie International Edition},
pages={11514--11516},
author={Schwarzer, Darius Daniel and Gritsch, Philipp J. and Gaich, Tanja}
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<dcterms:abstract xml:lang="eng">Experimental evidence was found to support an enzymatic [3,3]-sigmatropic rearrangement catalyzed by dimethylallyltryptophan (DMAT) synthase (see scheme). A bio-inspired system showed the feasibility of Cope rearrangement to the C-4 position of the indole nucleus. The tricyclic benzo[cd]indole core of welwitindolinones and dragmacidin E was synthesized using this transformation.</dcterms:abstract>
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