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Diels–Alder routes to angularly halogenated cis-fused bicyclic ketones: Readily accessible cyclynone intermediates
We have developed an efficient Lewis acid-catalyzed Diels–Alder route to a series of cis-fused bicyclic ketones bearing quaternary halogenation at the angular position. We have also developed a Diels–Alder based one-flask method for the regioselective preparation of TBS-protected 6-hydroxy tetralone...
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| Main Authors: | , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2010
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2936481/ https://ncbi.nlm.nih.gov/pubmed/20835369 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2010.06.135 |
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