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Nutt et al., 1984 - Google Patents

Synthesis of dihydromauritine A, a reduced cyclopeptide alkaloid

Nutt et al., 1984

Document ID
808506489962548667
Author
Nutt R
Chen K
Joullie M
Publication year
Publication venue
The Journal of Organic Chemistry

External Links

Snippet

The synthesis of the strained 14-membered cyclopeptide alkaloid derivative dihydromauritine A has been accomplished from L-proline via an SN2 displacement and three amide bond forming steps. The nucleophilic displacement involved a ß-bromopyrroline …
Continue reading at pubs.acs.org (other versions)

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    • C07K5/10Tetrapeptides
    • C07K5/1002Tetrapeptides with the first amino acid being neutral
    • C07K5/1005Tetrapeptides with the first amino acid being neutral and aliphatic
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    • C07K5/06139Dipeptides with the first amino acid being heterocyclic
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    • C07K1/061General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
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