par Roeland, Serge;Fuks, Robert 
Référence Synthetic communications, 16, 13, page (1693-1699)
Publication Publié, 1986-11
Référence Synthetic communications, 16, 13, page (1693-1699)
Publication Publié, 1986-11
Article révisé par les pairs
| Résumé : | The amidinoethylation of alcohols by their Michael-type addition to propenamidines takes place without the need of a basic catalyst. The effect of the basicity of the amidine and the nature of the alcohol on the course of the reaction is discussed. The reaction is assumed to proceed by an SN1 mechanism. © 1986, Taylor & Francis Group, LLC. All rights reserved. |
