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  Peptidsynthesen, LVI. Verwendung symmetrischer Boc-aminosäureanhydride

Flor, F., Birr, C., & Wieland, T. (1973). Peptidsynthesen, LVI. Verwendung symmetrischer Boc-aminosäureanhydride. Liebigs Annalen der Chemie, 1973(10), 1601-1605. doi:10.1002/jlac.197319731003.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-9B9E-5 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-9B9F-3
Genre: Journal Article

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LiebigsAnnChem_1973_1973_1601.pdf (Any fulltext), 310KB
 
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 Creators:
Flor, Friedlieb1, Author           
Birr, Christian1, Author           
Wieland, Theodor1, Author           
Affiliations:
1Max Planck Institute for Medical Research, Max Planck Society, ou_1125545              

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 Abstract: Symmetrische Boc-aminosäureanhydride werden aus den Natriumsalzen der Boc-aminosäuren in Tetrahydrofuran oder aus den Triäthylammoniumsalzen in Methylendichlorid mit Phosgen hergestellt und in situ mit verschiedenen Aminosäure- oder Peptid-methylestern zu Boc-peptidestern gekuppelt. Die Ausbeuten sind mit den mit gemischten Anhydriden erhaltenen vergleichbar (siehe Tabelle 1).

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Language(s): deu - German
 Dates: 1973-03-012006-01-251973-10-31
 Publication Status: Issued
 Pages: 5
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 Rev. Type: Peer
 Identifiers: DOI: 10.1002/jlac.197319731003
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Title: Liebigs Annalen der Chemie
Source Genre: Journal
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Publ. Info: Weinheim [Germany] : VCH Verlagsgesellschaft [etc.]
Pages: - Volume / Issue: 1973 (10) Sequence Number: - Start / End Page: 1601 - 1605 Identifier: ISSN: 0170-2041
CoNE: https://pure.mpg.de/cone/journals/resource/954928542197