Original and efficient method for the preparation of N-aminoamide pseudodipeptides in high optical purity
✍ Scribed by Nicolas Brosse; Arnaud Grandeury; Brigitte Jamart-Grégoire
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 63 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
N-Aminoamide pseudodipeptides ZAAC[CO-N(NPht)]-AAOR can be easily obtained via the Mitsunobu protocol by using a-hydroxyesters as alcohol partners and aminoacid phthaloyl hydrazide derivatives as acidic partners. The direct conversion of the phthaloyl group into tert-butyloxycarbonyl can be performed in a three-stage one-pot protocol.
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