A new protecting group for amines. Synthesis of anticapsin from L-tyrosine
β Scribed by Bennett C. Laguzza; Bruce Ganem
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 272 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
An acid and base-stable, nucleophile-resistant protecting group for primary amines and a-amino acids is described which has been used in a synthesis of the title compound.
π SIMILAR VOLUMES
Use of dimethylphosphinyl (Dmp) group as a side-chain phenolic OH protecting group of tyrosine in peptide synthesis was studied. The Dmp group is resistant to trifluoroacetic acid and hydrogenolysis and removed by fluoride ion or liquid HF. The formation of 3-benzyltyrosine from e-benzyl tyrosine in
A new reagent --4-nitro-l-H-pyrazole-l-[N, N'-bis(ten-butoxycarbonyl)]cmboxamidine --has been develolxd to effect the rapid a~l efficient synthesis of I~(~)-pmtected guanidin~ from and secendm3, amines. The reagent is a more eleclrophilic, sad comfy more derivative of the literature reagent l-H-pyra