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Sodium borohydride: A versatile reagent in the reductive N-monoalkylation of α-amino acids and α-amino methyl esters

VERARDO, Giancarlo
•
GEATTI, Paola
•
POL E
•
GIUMANINI A. G.
2002
  • journal article

Periodico
CANADIAN JOURNAL OF CHEMISTRY
Abstract
α-Amino acids and α-amino methyl esters are easily converted to their N-monoalkyl derivatives by a reductive condensation reaction using several carbonyl compounds in the presence of sodium borohydride. This reducing agent has shown a wide versatility with minor but essential procedural variations. The reaction allows the α-monodeuterium labeling of the new N-substituent by use of sodium borodeuteride.
DOI
10.1139/V02-083
WOS
WOS:000177192300005
Archivio
http://hdl.handle.net/11390/714654
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0036042072
Diritti
metadata only access
Soggetti
  • α-amino acid, α-amino...

Scopus© citazioni
27
Data di acquisizione
Jun 2, 2022
Vedi dettagli
Web of Science© citazioni
26
Data di acquisizione
Feb 25, 2024
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