Publikation: A Photoinduced Cyclization Cascade : Total Synthesis of (−)-Leuconoxine
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2015
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Chemistry : a European journal. 2015, 21(17), pp. 6355-6357. ISSN 0947-6539. eISSN 1521-3765. Available under: doi: 10.1002/chem.201500656
Zusammenfassung
A protecting-group-free and enantioselective total synthesis of the monoterpenoid indole alkaloid (-)-leuconoxine was accomplished. The key step comprises a novel photoinduced domino macrocyclization/transannular cyclization involving the Witkop cyclization, for which additional mechanistic evidence is provided. This process furnishes a diaza[5.5.6.6]fenestrane skeleton, which is a hitherto unprecedented structure element.
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PFAFFENBACH, Magnus, Tanja GAICH, 2015. A Photoinduced Cyclization Cascade : Total Synthesis of (−)-Leuconoxine. In: Chemistry : a European journal. 2015, 21(17), pp. 6355-6357. ISSN 0947-6539. eISSN 1521-3765. Available under: doi: 10.1002/chem.201500656BibTex
@article{Pfaffenbach2015Photo-32755,
year={2015},
doi={10.1002/chem.201500656},
title={A Photoinduced Cyclization Cascade : Total Synthesis of (−)-Leuconoxine},
number={17},
volume={21},
issn={0947-6539},
journal={Chemistry : a European journal},
pages={6355--6357},
author={Pfaffenbach, Magnus and Gaich, Tanja}
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<dcterms:abstract xml:lang="eng">A protecting-group-free and enantioselective total synthesis of the monoterpenoid indole alkaloid (-)-leuconoxine was accomplished. The key step comprises a novel photoinduced domino macrocyclization/transannular cyclization involving the Witkop cyclization, for which additional mechanistic evidence is provided. This process furnishes a diaza[5.5.6.6]fenestrane skeleton, which is a hitherto unprecedented structure element.</dcterms:abstract>
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