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

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