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A convergent, scalable and stereoselective synthesis of azole CYP51 inhibitors
The study and development of azole-based CYP51 inhibitors is an active area of research across disciplines of biochemistry, pharmacology and infectious disease. Support of in vitro and in vivo studies require the development of robust asymmetric routes to single enantiomer products of this class of...
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| Publicat a: | Tetrahedron Lett |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5777588/ https://ncbi.nlm.nih.gov/pubmed/29371747 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2017.09.070 |
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