enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Carvone - Wikipedia

    en.wikipedia.org/wiki/Carvone

    Carvone may be synthetically prepared from limonene by first treating limonene nitrosyl chloride. Heating this nitroso compound gives carvoxime. Treating carvoxime with oxalic acid yields carvone. [14] This procedure affords R-(−)-carvone from R-(+)-limonene. The major use of d-limonene is as a precursor to S-(+)-carvone. The large scale ...

  3. Levopropoxyphene - Wikipedia

    en.wikipedia.org/wiki/Levopropoxyphene

    Levopropoxyphene is an antitussive.It is an optical isomer of dextropropoxyphene.The racemic mixture is called propoxyphene.Only the dextro-isomer (dextropropoxyphene) has an analgesic effect; the levo-isomer appears to exert only an antitussive effect.

  4. Dextropropoxyphene - Wikipedia

    en.wikipedia.org/wiki/Dextropropoxyphene

    Dextropropoxyphene [5] is an analgesic in the opioid category, patented in 1955 [6] and manufactured by Eli Lilly and Company.It is an optical isomer of levopropoxyphene.It is intended to treat mild pain and also has antitussive (cough suppressant) and local anaesthetic effects.

  5. D-DOPA - Wikipedia

    en.wikipedia.org/wiki/D-DOPA

    Levo- and dextro- rotation refer to a molecule's ability to rotate planes of polarized light in one or the other direction. Whereas L -DOPA is moderately effective in the treatment of Parkinson's disease (PD) and dopamine-responsive dystonia (DRD) by stimulating the production of dopamine in the brain, D -DOPA is biologically inactive.

  6. Racemization - Wikipedia

    en.wikipedia.org/wiki/Racemization

    Plus and minus forms are called Dextrorotation and levorotation. [1] The D and L enantiomers are present in equal quantities, the resulting sample is described as a racemic mixture or a racemate. Racemization can proceed through a number of different mechanisms, and it has particular significance in pharmacology inasmuch as different ...

  7. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    An enantiomeric pair (S,S)- and (R,R)-ethambutol, along with the achiral stereoisomer called meso-form, it holds a diastereomeric relationship with the optically active stereoisomers. The activity of the drug resides in the (S,S)-enantiomer which is 500 and 12 fold more potent than the (R,R)-ethambutol and the meso-form. The drug had initially ...

  8. Dextromethorphan/bupropion - Wikipedia

    en.wikipedia.org/wiki/Dextromethorphan/bupropion

    [2] [3] It is taken as a tablet by mouth. [1] Side effects of dextromethorphan/bupropion include dizziness, headache, diarrhea, somnolence, dry mouth, sexual dysfunction, and hyperhidrosis, among others. [1] The mechanism of action of dextromethorphan/bupropion in the treatment of depression is unknown. [1]

  9. Enone–alkene cycloadditions - Wikipedia

    en.wikipedia.org/wiki/Enone–alkene_cycloadditions

    In 1908, it was reported that exposure of carvone to "Italian sunlight" for one year gives carvone-camphor. [2] Subsequent investigations demonstrated the utility of the photochemical [2+2] cycloaddition of enones to alkenes, requiring only "sunlight in California for 6.5 months". [3] [4]