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Synthesis of cis-Oriented Vicinal Diphenylethylenes through a Lewis Acid-Promoted Annulation of Oxotriphenylhexanoates
[Image: see text] This study explores the synthesis of cyclic cis-vicinal phenyl ethylenes from oxotriphenylhexanoates. The reaction is a BBr(3)-promoted cyclization of 1,6-ketoesters (1) to five-membered diketo compounds (2). The synthesis is interesting as it constitutes one of the few examples of...
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| Vydáno v: | J Org Chem |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Chemical
Society
2021
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8279482/ https://ncbi.nlm.nih.gov/pubmed/34138578 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.joc.1c00445 |
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