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Cited by 433

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Chemoselective Amide Ligations by Decarboxylative Condensations of N ‐Alkylhydroxylamines and α‐Ketoacids

Bode, Jeffrey W., Fox, Ryan M., Baucom, Kyle D.·2006·Angewandte Chemie International Edition

Abstract

Additive-free: The chemoselective amide-bond-forming ligation between N-alkylhydroxylamines and α-ketoacids requires no reagents and the only by-products are water and carbon dioxide. This process proceeds on unprotected peptide substrates without epimerization, and as such, this process has the potential to serve as a novel chemoselective ligation for the synthesis of peptides and complex materials.

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Crossref · 10.1002/anie.200503991

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Metadata

Authors
Bode, J. W., Fox, R. M., & Baucom, K. D.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2006-02-06
Volume
45
Issue
8
Pages
1248-1252
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2139411610
Cited by
433
References
1
FWCI
5.28
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Chemoselective Amide Ligations by Decarboxylative Condensations of N ‐Alkylhydroxylamines and α‐Ketoacids. https://app.cochat.ai/papers/10.1002/anie.200503991
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Bode, J. W., Fox, R. M., & Baucom, K. D. (2006). Chemoselective Amide Ligations by Decarboxylative Condensations of N ‐Alkylhydroxylamines and α‐Ketoacids. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200503991

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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.