Dedicated to Prof. Dr. Volker Jäger
Pactamycin, a potent antitumor and antimicrobial antibiotic, possesses a densely functionalized
cyclopentane core structure. This paper describes the concise synthesis of an advanced
intermediate for synthesizing the enantiomer of pactamycin that contains the cyclopentane
skeleton bearing all the necessary amino functions with correct stereochemistries.
Key words
natural product synthesis - pactamycin - aminocyclopentitol - oxime–olefin cycloaddition
- aziridines