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Total synthesis of biseokeaniamides A–C and late-stage electrochemically-enabled peptide analogue synthesis

The first total synthesis of cytotoxic cyanobacterial peptide natural products biseokeaniamides A–C is reported employing a robust solid-phase approach to peptide backbone construction followed by coupling of a key thiazole building block. To rapidly access natural product analogues, we have optimiz...

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Bibliografski detalji
Izdano u:Chem Sci
Glavni autori: Lin, Yutong, Malins, Lara R.
Format: Artigo
Jezik:Inglês
Izdano: The Royal Society of Chemistry 2020
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8162360/
https://ncbi.nlm.nih.gov/pubmed/34094328
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/d0sc03701j
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