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6-exo-trig Michael addition-lactonizations for catalytic enantioselective chromenone synthesis
The catalytic enantioselective 6-exo-trig Michael addition-lactonization of enone-acid substrates to form cis-chromenones with high diastereo- and enantiocontrol was developed using the commercially available isothiourea tetramisole. An acidic workup proved necessary to minimize product epimerizatio...
Autores principales: | Neyyappadath, Rifahath M., Cordes, David B., Slawin, Alexandra M. Z., Smith, Andrew D. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358503/ https://www.ncbi.nlm.nih.gov/pubmed/28133660 http://dx.doi.org/10.1039/c6cc10178j |
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