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Diastereoselective Dearomatization of Resorcinols Directed by a Lactic Acid Tether: Unprecedented Enantioselective Access to p-Quinols
[Image: see text] An operationally simple oxidative dearomatization of resorcinol derivatives is reported that employs an inexpensive chiral directing group. The method provides access to a variety of p-quinol derivatives in good yield and diastereoselectivity. A short reductive process affords 4-hy...
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| Main Authors: | , , |
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| Format: | Artigo |
| Language: | Inglês |
| Published: |
2004
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1360179/ https://ncbi.nlm.nih.gov/pubmed/15128229 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol0498592 |
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