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Synthesis of Substituted Chromanones: An Organocatalytic Aldol/oxa-Michael Reaction
[Image: see text] A diastereoselective organocatalytic aldol/oxa-Michael reaction has been developed to efficiently deliver medicinally relevant 2,3-ring substituted chromanones. Development of this synthetic strategy revealed an unexpected kinetic anti-Saytzeff elimination; an origin for the observ...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3164863/ https://ncbi.nlm.nih.gov/pubmed/20617821 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol101221c |
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