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A One‐Pot Total Synthesis of Crambin

Bang, Duhee, Kent, Stephen B. H.·2004·Angewandte Chemie International Edition

Abstract

Making up for lost time: The one-pot synthesis of crambin (see structure) with only a single final purification step gave the target protein of exceptional purity in only two days with an overall yield of ≈40 %. Three unprotected peptide segments were linked by native chemical ligation, and the polypeptide chain assumed its 3D structure without intermediate purification steps.

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Metadata

Authors
Bang, D., & Kent, S. B. H.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2004-04-28
Volume
43
Issue
19
Pages
2534-2538
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2138995597
Cited by
380
References
0
FWCI
4.70
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: A One‐Pot Total Synthesis of Crambin. https://app.cochat.ai/papers/10.1002/anie.200353540
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Bang, D., & Kent, S. B. H. (2004). A One‐Pot Total Synthesis of Crambin. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200353540

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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