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  2. Strecker amino acid synthesis - Wikipedia

    en.wikipedia.org/wiki/Strecker_amino_acid_synthesis

    The initial reaction product of 3-methyl-2butanone with sodium cyanide and ammonia is resolved by application of L-tartaric acid. In contrast, asymmetric Strecker reactions require no resolving agent. By replacing ammonia with (S)-alpha-phenylethylamine as chiral auxiliary the ultimate reaction product was chiral alanine. [6]

  3. Alkaloid - Wikipedia

    en.wikipedia.org/wiki/Alkaloid

    Medical use of alkaloid-containing plants has a long history, and, thus, when the first alkaloids were isolated in the 19th century, they immediately found application in clinical practice. [206] Many alkaloids are still used in medicine, usually in the form of salts widely used including the following: [ 14 ] [ 207 ]

  4. Medicinal chemistry - Wikipedia

    en.wikipedia.org/wiki/Medicinal_chemistry

    In the medicinal chemistry specialty areas associated with the design and synthesis of chemical libraries or the execution of process chemistry aimed at viable commercial syntheses (areas generally with fewer opportunities), training paths are often much more varied (e.g., including focused training in physical organic chemistry, library ...

  5. p-Toluenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/P-Toluenesulfonic_acid

    p-Toluenesulfonic acid (PTSA, pTSA, or pTsOH) or tosylic acid (TsOH) is an organic compound with the formula CH 3 C 6 H 4 SO 3 H. It is a white extremely hygroscopic solid that is soluble in water, alcohols, and other polar organic solvents. [6] The CH 3 C 6 H 4 SO 2 group is known as the tosyl group and is often abbreviated as Ts or Tos.

  6. Fischer indole synthesis - Wikipedia

    en.wikipedia.org/wiki/Fischer_indole_synthesis

    The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a (substituted) phenylhydrazine and an aldehyde or ketone under acidic conditions.

  7. Olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Olefin_metathesis

    In organic chemistry, olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes (olefins) by the scission and regeneration of carbon-carbon double bonds. [ 1 ] [ 2 ] Because of the relative simplicity of olefin metathesis, it often creates fewer undesired by-products and hazardous wastes than alternative ...

  8. Organic synthesis - Wikipedia

    en.wikipedia.org/wiki/Organic_synthesis

    Organic synthesis is an important chemical process that is integral to many scientific fields. Examples of fields beyond chemistry that require organic synthesis include the medical industry, pharmaceutical industry, and many more. Organic processes allow for the industrial-scale creation of pharmaceutical products.

  9. PHBV - Wikipedia

    en.wikipedia.org/wiki/PHBV

    PHBV find its application in controlled release of drugs, medical implants and repairs, specialty packaging, orthopedic devices and manufacturing bottles for consumer goods. It is also biodegradable which can be used as an alternative to non biodegradable plastics [ 9 ]