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note
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This strain has been deposited with the ATCC for registration.
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19
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0005211707
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note
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3CN (1.0 equiv), and the reaction was allowed to stir overnight at room temperature. Aqueous workup afforded the crude reductive amination product which was deprotected (TBAF in THF, then 1 N HCl in MeOH) according to standard procedures. The final targets 4a-n were purified to homogeneity by silica gel chromatography.
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20
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0027408378
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For other examples of syn-selective oxidation of triols, see (a) Jeong L.S., Shinazi R.F., Beach J.W., Kim H.O., Nampalli S. J. Med. Chem. 36:1993;181 (b) Stache U., Radscheit K., Haede W., Fritsch W. Liebigs Ann. Chem. 2:1982;342.
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0019977893
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For other examples of syn-selective oxidation of triols, see (a) Jeong L.S., Shinazi R.F., Beach J.W., Kim H.O., Nampalli S. J. Med. Chem. 36:1993;181 (b) Stache U., Radscheit K., Haede W., Fritsch W. Liebigs Ann. Chem. 2:1982;342.
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note
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-) 534.
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23
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0005151290
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note
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The fungal strains used in this study were obtained from the American Type Culture Collection. MICs were determined according to National Committee for Clinical Laboratory Standards (NCCLS); NCCLS Document M27-A; NCCLS: Villanova, PA, 1997.
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