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Benign Synthesis of Thiazolo-androstenone Derivatives as Potent Anticancer Agents
An unprecedented reaction of thiourea derivatives with 6β-bromoandrostenedione has been discovered for the formation of aminothiazolo-androstenones via a simple, safer, cascade protocol that enables the syntheses of novel molecules by using readily available reagents. The reaction mechanism of produ...
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| Publicado no: | Org Lett |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6441354/ https://ncbi.nlm.nih.gov/pubmed/30204455 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.8b02587 |
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