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Cited by 133Chemical Synthesis and AnalysisSynthesis and Reactivity of Sulfur-Containing CompoundsSulfur-Based Synthesis Techniques

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Thiopeptide Synthesis. α-Amino Thionoacid Derivatives of Nitrobenzotriazole as Thioacylating Agents

Shalaby, M. Ashraf, Grote, Christopher W., Rapoport, Henry·1996·The Journal of Organic Chemistry
DOI 10.1021/jo961245q
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Abstract

ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTThiopeptide Synthesis. α-Amino Thionoacid Derivatives of Nitrobenzotriazole as Thioacylating AgentsM. Ashraf Shalaby, Christopher W. Grote, and Henry RapoportView Author Information Department of Chemistry and Materials Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720 Cite this: J. Org. Chem. 1996, 61, 25, 9045–9048Publication Date (Web):December 13, 1996Publication History Received2 July 1996Published online13 December 1996Published inissue 1 January 1996https://pubs.acs.org/doi/10.1021/jo961245qhttps://doi.org/10.1021/jo961245qbrief-reportACS PublicationsCopyright © 1996 American Chemical SocietyRequest reuse permissionsArticle Views2990Altmetric-Citations113LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Chemical reactions,Monomers,Peptides and proteins,Reaction products,Reagents Get e-Alerts

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  • This macrolactonization protocol avoids the harsh conditions typically associated with traditional macrolactonization strategies.

    “This protocol avoids the harsh conditions typically associated with traditional marcrolactonization strategies.50”

    From Ynamide Coupling Reagents: Origin and Advances (2024) · cites this paper as [50]

Citations

Cites

No references could be resolved yet.

Research works printed but not linked: 20

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  6. Guthrie D. J. S., 1986, Int. J. Pept. Protein Res., 28, 208, 10.1111/j.1399-3011.1986.tb03249.x · DOI
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  17. Brutsche, 1992, Liebigs Ann. Chem., 921, 10.1002/jlac.1992199201152 · DOI
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  19. Katritzky A. R., 1991, J. Tetrahedron, 47, 2683, 10.1016/S0040-4020(01)87080-0 · DOI
  20. Anderson G. W., 1967, J. Am. Chem. Soc., 89, 5012, 10.1021/ja00995a032 · DOI

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Metadata

Authors
Shalaby, M. A., Grote, C. W., & Rapoport, H.
Affiliations
Lawrence Berkeley National Laboratory (US)
Venue
The Journal of Organic Chemistry
Publisher
American Chemical Society (ACS)
Published
1996-01-01
Volume
61
Issue
25
Pages
9045-9048
ISSN
  • 0022-3263 (ISSN-L)
  • 1520-6904
DOI
10.1021/jo961245q
OpenAlex
W1993309394
Cited by
133
References
0
Citations by year
2026: 4 · 2025: 4 · 2024: 12 · 2023: 5 · 2022: 8 · 2021: 5 · 2020: 4 · 2019: 9 · 2018: 6 · 2017: 2 · 2016: 3 · 2015: 6 · 2014: 6 · 2013: 7 · 2012: 2
FWCI
1.53
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Organic Chemistry (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Analysis
  • Physical Sciences › Chemistry › Organic Chemistry › Synthesis and Reactivity of Sulfur-Containing Compounds
  • Physical Sciences › Chemistry › Organic Chemistry › Sulfur-Based Synthesis Techniques
Keywords
thioacylation, peptide synthesis reagents

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