Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 1921-1933 |
| Seitenumfang | 13 |
| Fachzeitschrift | Organic and Biomolecular Chemistry |
| Jahrgang | 2 |
| Ausgabenummer | 13 |
| Publikationsstatus | Veröffentlicht - 7 Juli 2004 |
| Extern publiziert | Ja |
Abstract
An indium mediated procedure has been developed for the allylation of activated O-functionalised oximes and nitriles as exemplified by a variety of glyoxylate derivatives. This method gives the corresponding free (or protected) amine in a one pot-process. The method is regiospecific and is carried out under remarkably mild conditions so that even oxime esters can be subjected to the typical reaction conditions.
ASJC Scopus Sachgebiete
- Biochemie, Genetik und Molekularbiologie (insg.)
- Biochemie
- Chemie (insg.)
- Physikalische und Theoretische Chemie
- Chemie (insg.)
- Organische Chemie
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in: Organic and Biomolecular Chemistry, Jahrgang 2, Nr. 13, 07.07.2004, S. 1921-1933.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Indium mediated allylation of glyoxylate oxime ethers, esters and cyanoformates
AU - Ritson, Dougal J.
AU - Cox, Russell J.
AU - Berge, John
PY - 2004/7/7
Y1 - 2004/7/7
N2 - An indium mediated procedure has been developed for the allylation of activated O-functionalised oximes and nitriles as exemplified by a variety of glyoxylate derivatives. This method gives the corresponding free (or protected) amine in a one pot-process. The method is regiospecific and is carried out under remarkably mild conditions so that even oxime esters can be subjected to the typical reaction conditions.
AB - An indium mediated procedure has been developed for the allylation of activated O-functionalised oximes and nitriles as exemplified by a variety of glyoxylate derivatives. This method gives the corresponding free (or protected) amine in a one pot-process. The method is regiospecific and is carried out under remarkably mild conditions so that even oxime esters can be subjected to the typical reaction conditions.
UR - http://www.scopus.com/inward/record.url?scp=3142714522&partnerID=8YFLogxK
U2 - 10.1039/b402764g
DO - 10.1039/b402764g
M3 - Article
AN - SCOPUS:3142714522
VL - 2
SP - 1921
EP - 1933
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
SN - 1477-0520
IS - 13
ER -