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Facile Chemoselective Synthesis of Dehydroalanine-Containing Peptides

Okeley, Nicole M., Zhu, Yantao, van der Donk, Wilfred A.·2000·Organic Letters

Abstract

Useful methodology is described for the synthesis of dehydroalanine residues (II) within peptides. The unnatural amino acid (Se)-phenylselenocysteine (I) can be incorporated into growing peptide chains via standard peptide synthesis procedures. Subsequent oxidative elimination affords a dehydroalanine at the desired position. The oxidation conditions are mild and tolerate functionalities commonly found in peptides, including variously protected cysteine residues. To illustrate its utility, cyclic lanthionines have been synthesized by this method.

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Metadata

Authors
Okeley, N. M., Zhu, Y., & van der Donk, W. A.
Venue
Organic Letters
Published
2000-10-24
Volume
2
Issue
23
Pages
3603-3606
ISSN
  • 1523-7052 (ISSN-L)
  • 1523-7060
OpenAlex
W2047654005
Cited by
165
References
0
FWCI
2.03
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Facile Chemoselective Synthesis of Dehydroalanine-Containing Peptides. https://app.cochat.ai/papers/10.1021/ol006485d
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Okeley, N. M., Zhu, Y., & van der Donk, W. A. (2000). Facile Chemoselective Synthesis of Dehydroalanine-Containing Peptides. Organic Letters. https://doi.org/10.1021/ol006485d

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.