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  • Organic Chemistry  (2)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 74 (1991), S. 326-330 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crystal Structure of a Thiazolorifamycine: Rifamycine PThe crystal structure of a natural thiazolorifamycin, rifamycin P, as an adduct with EtOH and H2O, has been determined by X-ray crystallography by a combination of direct methods and Patterson techniques. Block-diagonal least-squares refinement using 5996 independent reflections and 1475 parameters led to an R factor of 0.092 (two independent molecules of rifamycin P). The middle part of the ansa chain, essential for activity against the bacterial DNA-dependent RNA polymerase (DDRP) resembles that of active rifamycins. The four OH groups lie on the same side of the molecule and are almost in the same plane. Interatomic distances between the O-atoms agree well with a spatial model derived from X-ray studies, performed on semisynthetic active rifamycins.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Optical Isomers of Naftidrofuryl( = 2-(Diethylamino)ethyl 2-[(Naphth-1-yl)methyl]-3-(tetrahydrofur-2-yl)propanoate)The four optical isomers of naftidrofuryl (1) were prepared in two ways, by separation and resolution of the two diastereoisomeric racemates and by synthesis from the enantiomers of tetrahydrofuran-2-methanol (6); see Scheme}. The absolute configuration of one of the isomer as a tartrate monohydrate was established by X-ray crystallography thus allowing the deduction of the absolute configurations of the other three optical isomers.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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