| Synthesis of phosphonamidate peptides by Staudinger reactions of silylated phosphinic acids and esters. | |
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MedLine Citation:
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PMID: 20830364 Owner: NLM Status: In-Process |
Abstract/OtherAbstract:
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The Staudinger reaction of unprotected azido-peptides with silylated phosphinic acids and esters on the solid support offers a straightforward acid-free entry to different phosphonamidate peptide esters or acids under mild conditions in high purity and yield. |
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Authors:
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Ina Wilkening; Giuseppe del Signore; Christian P R Hackenberger |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2010-09-07 |
Journal Detail:
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Title: Chemical communications (Cambridge, England) Volume: 47 ISSN: 1364-548X ISO Abbreviation: Chem. Commun. (Camb.) Publication Date: 2011 Jan |
Date Detail:
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Created Date: 2010-12-08 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9610838 Medline TA: Chem Commun (Camb) Country: England |
Other Details:
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Languages: eng Pagination: 349-51 Citation Subset: IM |
Affiliation:
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Freie Universität Berlin, Institut für Chemie und Biochemie, Takustr. 3, 14195 Berlin, Germany. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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