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Regioselectivity of the S(E)Ar-based cyclizations and S(E)Ar-terminated annulations of 3,5-unsubstituted, 4-substituted indoles
Indole-3,4- and 4,5-fused carbo- and heterocycles are ubiquitous in bioactive natural products and pharmaceuticals, and hence, a variety of synthetic approaches toward such compounds have been developed. Among these, cyclization and annulation of 3,5-unsubstituted, 4-substituted indoles involving an...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Beilstein-Institut
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919422/ https://www.ncbi.nlm.nih.gov/pubmed/35330778 http://dx.doi.org/10.3762/bjoc.18.33 |