Two synthetic strategies for the generation of differentially protected, chiral tri-amino acids have been developed. The first strategy is based on the reductive amination of a serine-derived oxazolidine aldehyde with mono N-protected ethylenediamine. The second approach involves reductive alkylatio
✦ LIBER ✦
Synthesis of orthogonally protected azepane β-amino ester enantiomers
✍ Scribed by Brigitta Kazi; Loránd Kiss; Enikő Forró; Ferenc Fülöp
- Book ID
- 104097088
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 212 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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