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  • Organic Chemistry  (3)
  • iron phosphine  (2)
  • Wiley-Blackwell  (3)
  • American Chemical Society
  • Cell Press
  • 1990-1994  (3)
  • 1
    ISSN: 0899-0042
    Keywords: chirality ; fluoxetine ; norfluoxetine ; desipramine ; iprindole ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The antidepressant fluoxetine (FLU) and its N-demethylated metabolite, norfluoxetine (NFLU), each contains a chiral center. The combination of FLU and desipramine (DMI), another antidepressant, has been reported to be useful in treatment of depression, to dramatically increase plasma levels of DMI and also to produce more rapid β-adrenergic receptor down-regulation in brain than caused by DMI alone. We have now begun studies on the effects of this drug combination on the levels of FLU and NFLU enantiomers in the rat. In addition, the combination of FLU and iprindole (IPR) was also investigated. Male Sprague-Dawley rats were treated intraperitoneally with either normal saline vehicle, DMI (5 mg/kg/day), (R,S)-FLU (10 mg/kg/day) or DMI (5 mg/kg/day) + (R,S)-FLU (10 mg/kg/day) for 4 days. Following the last treatment, 24 h urine samples were collected. Rats were sacrificed and brains were removed. For the IPR study, rats were pretreated with either saline or IPR-HCl (11.2 mg/kg) and then treated 1 h later with (R,S)-FLU. After 5 h, the rats were sacrificed and brains were removed. Brain and urine samples were analyzed by gas chromatography with electron-capture detection for free (R)- and (S)-FLU and (R)- and (S)-NFLU after extraction and reaction with (-)-(S)-N-(trifluoroacetyl)prolyl chloride. The results from the brains of the rats treated with DMI/FLU indicate that levels of the enantiomers of both FLU and NFLU were significantly increased over those seen in the animals receiving (R,S)-FLU alone. In the IPR/FLU treated rats, an increase in the brain levels of both (R)- and (S)-FLU was noted when compared with rats receiving (R,S)-FLU alone; however, there appeared to be no increase in the brain levels of NFLU enantiomers. © 1994 Wiley-Liss, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 4 (1990), S. 543-549 
    ISSN: 0268-2605
    Keywords: Borohydride ; iron phosphine ; organoiron ; NMR spectroscopy ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: FeH(DMPE)2(BH4) [DMPE = 1,2-bis(dimethylphosphino)ethane] is a stable, diamagnetic complex which can be synthesized readily by borohydride reduction of FeH(DMPE)2Cl or by treatment of Fe(DMPE)2H2 with borane. The complex contains an unsupported B—H—Fe hydrogen bridge. Analogous complexes with bulkier ligands, FeH(DEPE)2(BH4), [DEPE = 1,2-bis(diethylphosphino)ethane] and FeH(DPrPE)2(BH4) [DPrPE = 1,2-bis(di-n-propylphosphino)ethane], are less stable. In all complexes, in solution the borohydride ligand undergoes rapid internal motion, with all four boron-bound hydrogens interchanging environments. The barriers for BH4 reorientation (measured by NMR spectroscopy) are in the sequence FeH(DMPE)2(BH)4 〉 FeH(DEPE)2(BH)4 〉 FeH(DPrPE)2(BH4).
    Additional Material: 2 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 4 (1990), S. 551-556 
    ISSN: 0268-2605
    Keywords: Metal hydride ; iron phosphine ; organoiron ; NMR spectroscopy ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Syntheses and properties of the iron bisphosphinoethane complexes FeH2(PP)2 and FeHCl(PP)2[PP=R2PCH2CH2CH2PR2, where R=Me (PP=DMPE), Et(PP=DEPE), and n-Pr (PP=DprPE)] are reported. The complexes can be formed by reduction of the corresponding dichlorides FeCl2(PP)2 with lithium aluminium hydride in THF solution provided that ethanol or more acidic reagents are not employed during the reaction work-up. The dihydrides are notably basic compounds and can be protonated reversibly by alcohols.The dihydrides exist as equilibrating mixtures of cis and trans isomers in solution. The cis isomers of each of the dihydrides are fluxional on the NMR timescale and NMR studies indicate that the interconversion of cis isomers does not necessarily proceed via the trans isomer.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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