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  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. Optical rotation - Wikipedia

    en.wikipedia.org/wiki/Optical_rotation

    Dextrorotation and laevorotation (also spelled levorotation) [1] [2] in chemistry and physics are the optical rotation of plane-polarized light.From the point of view of the observer, dextrorotation refers to clockwise or right-handed rotation, and laevorotation refers to counterclockwise or left-handed rotation.

  4. 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 ...

  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. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    Structures of the two enantiomeric forms (S left, R right) of mecoprop Enantiomers of citalopram. The top is (R)-citalopram and the bottom is -citalopram. An example of such an enantiomer is the sedative thalidomide, which was sold in a number of countries around the world from 1957 until 1961. It was withdrawn from the market when it was found ...

  7. Decamethyldizincocene - Wikipedia

    en.wikipedia.org/wiki/Decamethyldizincocene

    Both (η 5-C 5 Me 5)ZnEt and decamethyldizincocene are produced from the reaction between Zn(η 5-C 5 Me 5) 2 and ZnEt 2. The relative amounts depend on reaction conditions, which can be optimized to favor one or the other. [2] For instance, if this reaction is conducted in pentane at -40 °C, (η 5-C 5 Me 5)ZnEt is the sole product.

  8. The Best Zinc Oxide Sunscreens to Safely Protect Your Skin - AOL

    www.aol.com/lifestyle/best-zinc-oxide-sunscreens...

    Choose from zinc sunscreens for your face, body, babies, and more. Have some (safe) fun in the sun with these dermatologist-approved zinc oxide sunscreens. Choose from zinc sunscreens for your ...

  9. Organozinc chemistry - Wikipedia

    en.wikipedia.org/wiki/Organozinc_chemistry

    The reaction is effected with zinc. The key zinc-intermediate formed is a carbenoid (iodomethyl)zinc iodide which reacts with alkenes to afford the cyclopropanated product. The rate of forming the active zinc species is increased via ultrasonication since the initial reaction occurs at the surface of the metal.

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