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Cited by 512

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

An Efficient Fmoc‐SPPS Approach for the Generation of Thioester Peptide Precursors for Use in Native Chemical Ligation

Open access
Blanco‐Canosa, Juan B., Dawson, Philip E.·2008·Angewandte Chemie International Edition

Abstract

Intramolecular activation of C-terminal peptides: Mildly activated N-acylurea peptides are readily formed on the solid support following chain assembly, avoiding over-activation of the C-terminus. The utility of these peptides is demonstrated by the native chemical ligation of unprotected peptides (see scheme; R=amino acid side chain).

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Crossref · 10.1002/anie.200705471

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Metadata

Authors
Blanco‐Canosa, J. B., & Dawson, P. E.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2008-08-20
Volume
47
Issue
36
Pages
6851-6855
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2161815395
Cited by
512
References
1
FWCI
8.44
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: An Efficient Fmoc‐SPPS Approach for the Generation of Thioester Peptide Precursors for Use in Native Chemical Ligation. https://app.cochat.ai/papers/10.1002/anie.200705471
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Blanco‐Canosa, J. B., & Dawson, P. E. (2008). An Efficient Fmoc‐SPPS Approach for the Generation of Thioester Peptide Precursors for Use in Native Chemical Ligation. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200705471

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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.