
Bioorganic and Medicinal Chemistry Letters p. 315 - 318 (1996)
Update date:2022-08-02
Topics:
Fobian
D'Avignon
Moeller
A facile route for the synthesis of peptide building blocks that constrain the peptide backbone with a 1,4-diazabicyclo[4.3.0]nonane ring skeleton is reported. The synthesis employed an anolic amide oxidation based approach for generating a functionalized proline derivative, and then utilized the derivative as a general substrate for rapidly assembling the bicyclic ring system.
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