Notizen: Einfache, schonende Synthese von Aminosäuremethyl- und benzylestern.-Reference-Cited by-同舟云学术

Notizen: Einfache, schonende Synthese von Aminosäuremethyl- und benzylestern.

Published:1976-08-01 Issue:8 Volume:31 Page:1157-1158
ISSN:1865-7117
Container-title:Zeitschrift für Naturforschung B
language:en
Short-container-title:

Author:

Weber U.¹

Affiliation:

1. Physiologisch-chemisches Institut, Universität Tübingen

Abstract

Methyl- and benzylesters of acid labile amino acids are obtained as their hydrochlorides or BF3-complexes by reaction of the N-protected amino acid with benzylalcohol (methanol), DCC, HOBt and pyridine and subsequent cleavage of the N-protection group by HCl in acetic acid or bortrifluorideetherate in acetic acid.

Publisher

Walter de Gruyter GmbH

Subject

General Chemistry

Link

https://www.degruyter.com/document/doi/10.1515/znb-1976-0835/pdf

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Activation of carboxylic acids by pyrocarbonates;International Journal of Peptide and Protein Research;2009-01-12

2. Second supplementary list of amino-acid derivatives useful in peptide synthesis;International Journal of Peptide and Protein Research;2009-01-12

3. Hydrogenolytic debenzylation of sulfur-containing peptides;International Journal of Peptide and Protein Research;2009-01-12

4. Preparation of Esters;Compendium of Organic Synthetic Methods;2006-11-22

5. Der 2,4,6-Triisopropylbenzolsulfonyl(Tip)-Rest, eine neue Schutzgruppe für die Guanidinofunktion von Arginin / The 2,4,6-Triisopropylbenzenesulfonyl Residue, a New Protecting Group for the Guanidino Function of Arginine;Zeitschrift für Naturforschung B;1987-12-01