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A concise and sequential synthesis of the nitroimidazooxazole based drug, Delamanid and related compounds
A concise, protection-group free and sequential route has been developed for the synthesis of the nitroimidazole based FDA-approved multi-drug resistant anti-tuberculosis drug, Delamanid and anti-leishmanial lead candidate VL-2098. The synthesis required chiral epoxides (11 and 17) as key intermedia...
Autores principales: | Sharma, Sumit, Anand, Radhika, Cham, Pankaj Singh, Raina, Sushil, Vishwakarma, Ram. A., Singh, Parvinder Pal |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053479/ https://www.ncbi.nlm.nih.gov/pubmed/35521460 http://dx.doi.org/10.1039/d0ra01662d |
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