Amidoethylation of anthracene hydride by n-aroylaziridines: inner-sphere single electron transfer (SET) and radical coupling confirmed
Regioselectivity (near 1:1) of substitutive ring opening of 1-benzoyl-2-methylaziridine by anthracene hydride is incompatible with common nucleophilic attack and thus confirms the radical coupling path.
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| Main Authors: | , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
1998
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| In: |
Journal of chemical research online. Synopses
Year: 1998, Issue: 10, Pages: 646-647 |
| ISSN: | 1364-5560 |
| DOI: | 10.1039/A804044C |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1039/A804044C Verlag, lizenzpflichtig, Volltext: https://pubs.rsc.org/en/content/articlelanding/1998/jc/a804044c 
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| Author Notes: | P.-Y. Lin, H. Stamm |
| Summary: | Regioselectivity (near 1:1) of substitutive ring opening of 1-benzoyl-2-methylaziridine by anthracene hydride is incompatible with common nucleophilic attack and thus confirms the radical coupling path. |
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| Item Description: | Gesehen am 11.07.2023 |
| Physical Description: | Online Resource |
| ISSN: | 1364-5560 |
| DOI: | 10.1039/A804044C |