What amino acid is formed using the n-phthalimidomalonic ester synthesis when the following alkyl halides are used in the third step?.

Respuesta :

Threre are two amino acid is formed using the n-phthalimidomalonic ester synthesis when the following alkyl halides are used in the third step -

a. leucine

b. methionine

What is Gabriel malonic ester synthesis?

  • A reaction that enables us to generate amino acids is the Gabriel synthesis, also referred to as the Gabriel malonic ester synthesis.
  • We can convert primary alkyl halides into primary amines using this procedure.
  • Remember that 19 of the 20 amino acids are actually primary amines.

Who should not take methionine?

  • Supplemental methionine shouldn't be used by people with the genetic condition homocystinuria type I.
  • Methionine can become more homocysteine if you take methionine supplements without getting enough folic acid, vitamin B-6, or vitamin B-12. Your risk of heart disease could rise as a result.

What does leucine do in the body?

  • Leucine is an essential amino acid for protein synthesis. Additionally, similarly to other amino acids, the carbon skeleton of leucine can be used to generate ATP.
  • However, leucine can also regulate several cellular processes such as protein synthesis, tissue regeneration, and metabolism.

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The complete question is -

What amino acid is formed using the N-phthalimidomalonic ester synthesis when the following alkyl halides are used in the third step?

a. Ch3Ch(Ch3)Ch2-Br

b. Ch3SCh2Ch2-Br

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