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• W2142754319 abstract "A series of lipophilic 2-substituted 5,7-di-tert-butylbenzoxazoles was prepared in average yields by the reaction of 3,5-di-tert-butyl-1,2-benzoquinone with amino acids and dipeptides bearing N-terminal glycine. Dipeptides having other N-terminal amino acids undergo oxidative deamination. 5,7-Di-tert-butylbenzoxazoles have shown activity against Mycobacterium tuberculosis and some nontuberculous strains where isoniazid has been inactive. Antifungal activity was mediocre." @default.
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• W2142754319 date "2005-08-31" @default.
• W2142754319 modified "2023-10-10" @default.
• W2142754319 title "Highly Lipophilic Benzoxazoles with Potential Antibacterial Activity" @default.
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• W2142754319 doi "https://doi.org/10.3390/10070783" @default.
• W2142754319 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6147629" @default.
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