Publikation: Intramolecular Cobalt-Catalyzed [2+2+2] Cycloaddition of O-Protected Diyne-Cyanohydrins
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2010
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Synlett. 2010, 2010(07), pp. 1051-1054. ISSN 0936-5214. Available under: doi: 10.1055/s-0029-1219572
Zusammenfassung
O-Protected cyanohydrins were found to serve as a source of the nitrile within the intramolecular cobalt-mediated [2+2+2] cycloaddition to pyridines. Several 6-substituted 1,2,3,4,7,8,9,10-octahydrophenanthridines were synthesized using this cycloaddition of diyne-cyanohydrins. By introduction a TMS group a divergent way to such phenanthridine derivatives was elaborated.
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540 Chemie
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cyanohydrin, cycloaddition, pyridines, alkynes, heterocycles
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MEISSNER, Anja, Ulrich GROTH, 2010. Intramolecular Cobalt-Catalyzed [2+2+2] Cycloaddition of O-Protected Diyne-Cyanohydrins. In: Synlett. 2010, 2010(07), pp. 1051-1054. ISSN 0936-5214. Available under: doi: 10.1055/s-0029-1219572BibTex
@article{Meiner2010Intra-12587,
year={2010},
doi={10.1055/s-0029-1219572},
title={Intramolecular Cobalt-Catalyzed [2+2+2] Cycloaddition of O-Protected Diyne-Cyanohydrins},
number={07},
volume={2010},
issn={0936-5214},
journal={Synlett},
pages={1051--1054},
author={Meißner, Anja and Groth, Ulrich}
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<dcterms:abstract xml:lang="eng">O-Protected cyanohydrins were found to serve as a source of the nitrile within the intramolecular cobalt-mediated [2+2+2] cycloaddition to pyridines. Several 6-substituted 1,2,3,4,7,8,9,10-octahydrophenanthridines were synthesized using this cycloaddition of diyne-cyanohydrins. By introduction a TMS group a divergent way to such phenanthridine derivatives was elaborated.</dcterms:abstract>
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