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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

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✦ 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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