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A Combined Experimental and Computational Investigation on the Unusual Molecular Mechanism of the Lossen Rearrangement Reaction Activated by Carcinogenic Halogenated Quinones
[Image: see text] The classic Lossen rearrangement is a well-known reaction describing the transformation of an O-activated hydroxamic acid into the corresponding isocyanate. In this study, we found that chlorinated benzoquinones (C(n)BQ) serve as a new class of agents for the activation of benzohyd...
Sparad:
| I publikationen: | J Org Chem |
|---|---|
| Huvudupphovsmän: | , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
American Chemical
Society
2014
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4285140/ https://ncbi.nlm.nih.gov/pubmed/25470188 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo5022713 |
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