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A Mild, Diastereoselective Construction of Cyclic and Spirocyclic Ketals Employing a Tandem Photoisomerization/Cyclization Tactic
[Image: see text] The cyclization of trans-δ-hydroxy enones to cyclic mixed ketals routinely requires superstoichiometric strong acid. By operating under a photoisomerization regime, the cyclization of trans-δ-hydroxy enones proceeds under catalytic Brønsted acid to provide cyclic ketals or unsatura...
Tallennettuna:
| Julkaisussa: | Org Lett |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American
Chemical Society
2014
|
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4295796/ https://ncbi.nlm.nih.gov/pubmed/25489978 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol503116q |
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