In Situ-Generated Niobium-Catalyzed Synthesis of 3‑Pyrroline Derivatives via Ring-Closing Metathesis Reactions
An active in situ-generated Nb complex was used as a catalyst in the ring-closing metathesis reaction of N,N-diallyl-p-toluenesulfonamide to afford the corresponding 3-pyrroline derivative. The Nb complex was formed from NbCl5, trimethylsilyl chloride, Zn, and PhCHCl2 in tetrahydrofuran. The Nb comp...
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Published in | ACS omega Vol. 3; no. 8; pp. 8865 - 8873 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
31.08.2018
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Online Access | Get full text |
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Summary: | An active in situ-generated Nb complex was used as a catalyst in the ring-closing metathesis reaction of N,N-diallyl-p-toluenesulfonamide to afford the corresponding 3-pyrroline derivative. The Nb complex was formed from NbCl5, trimethylsilyl chloride, Zn, and PhCHCl2 in tetrahydrofuran. The Nb complex displayed high catalytic activity toward ring-closing metathesis reactions. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2470-1343 2470-1343 |
DOI: | 10.1021/acsomega.8b01642 |