Site-selective conversion of azido groups at carbonyl α-positions into oxime groups leading triazide to a triple click conjugation scaffold.
Chem Commun (Camb)
; 55(13): 1891-1894, 2019 Feb 07.
Article
em En
| MEDLINE
| ID: mdl-30569047
ABSTRACT
This paper reports the selective conversion of alkyl azido groups at the carbonyl α-position into oximes through ß-elimination of dinitrogen, followed by transoximation. With this method and diazo conversion, a triazido molecule was transformed into a triple click conjugation scaffold allowing one-pot four-component coupling.
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1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Chem Commun (Camb)
Ano de publicação:
2019
Tipo de documento:
Article