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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. Chirality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(chemistry)

    Two enantiomers of a generic amino acid that are chiral (S)-Alanine (left) and (R)-alanine (right) in zwitterionic form at neutral pH. In chemistry, a molecule or ion is called chiral (/ ˈ k aɪ r əl /) if it cannot be superposed on its mirror image by any combination of rotations, translations, and some conformational changes.

  4. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    Louis Pasteur - pioneering stereochemist. Chirality can be traced back to 1812, when physicist Jean-Baptiste Biot found out about a phenomenon called "optical activity." [10] Louis Pasteur, a famous student of Biot's, made a series of observations that led him to suggest that the optical activity of some substances is caused by their molecular asymmetry, which makes nonsuperimposable mirror ...

  5. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    Chirality (/ k aɪ ˈ r æ l ɪ t i /) is a property of asymmetry important in several branches of science. The word chirality is derived from the Greek χείρ ( kheir ), "hand", a familiar chiral object.

  6. Sinistral and dextral - Wikipedia

    en.wikipedia.org/wiki/Sinistral_and_dextral

    Other disciplines use different terms (such as dextro-and laevo-rotary in chemistry, or clockwise and anticlockwise in physics) or simply use left and right (as in anatomy). Relative direction and chirality are distinct concepts.

  7. Optical rotation - Wikipedia

    en.wikipedia.org/wiki/Optical_rotation

    There is no strict relationship between the R/S, the D/L, and (+)/(−) designations, although some correlations exist. For example, of the naturally occurring amino acids, all are L, and most are (S). For some molecules the (R)-enantiomer is the dextrorotary (+) enantiomer, and in other cases it is the levorotary (−) enantiomer. The ...

  8. Racemic mixture - Wikipedia

    en.wikipedia.org/wiki/Racemic_mixture

    A single Adderall dose combines the neutral sulfate salts of dextroamphetamine and amphetamine, with the dextro isomer of amphetamine saccharate and D/L-amphetamine aspartate monohydrate. The original Benzedrine was a racemic mixture, and isolated dextroamphetamine was later introduced to the market as Dexedrine.

  9. Monoterpene - Wikipedia

    en.wikipedia.org/wiki/Monoterpene

    Carvone is a monoterpenoid. Hinokitiol is a monoterpenoid, a tropolone derivative. Linalool is an acyclic monoterpenoid. Bicyclic monoterpenes include carene, ...