81575-55-5Relevant academic research and scientific papers
Simple and rapid p-methoxybenzylation of hydroxy and amide groups at room temperature by NaOt-Bu and DMSO
Hamada, Shohei,Sugimoto, Koichi,Iida, Masashi,Furuta, Takumi
supporting information, (2019/11/13)
The p-methoxybenzylation of hydroxy and amide groups by p-methoxybenzyl chloride utilizing NaOt-Bu in DMSO is described. p-Methoxybenzylation of sterically hindered menthol using NaOt-Bu in DMSO proceeded faster than the commonly used methods which use Na
Synthesis of amides from imines using Et3SiH/Zn system
Ghaffarzadeh, Mohammad,Heidarifard, Somaye,Faraji, Fereshteh,Joghan, Somaye Shahrivari
experimental part, p. 103 - 107 (2012/05/05)
A simple and efficient approach for the synthesis of amides by the reaction of imines and acyl chlorides in the presence of Et3SiH/Zn system in THF at ambient temperature is reported. Mild reaction conditions, good yields of products, short reaction time and operational simplicity are the advantages of this procedure. Copyright
A new method for the synthesis of amides from imines
Ghaffarzadeh, Mohammad,Joghan, Somaye Shahrivari,Faraji, Fereshteh
experimental part, p. 203 - 206 (2012/03/07)
An efficient and straightforward method for the synthesis of amides by the reaction of imines and anhydrides in the presence of Et3SiH/Zn is reported. Mild reaction conditions, good yields of products, short reaction times, and operational simplicity are advantages of this procedure.
Bioorganic Studies: Part IV - Reductive N-Acylation of Imines Using 3,5-Dicarbethoxy-2,6-dimethyl-1,4-dihydropyridine as NADH Model
Singh, Serjinder,Sharma, Vijay K.
, p. 1087 - 1088 (2007/10/02)
A one-step reductive acetylation of imines (II) using 3,5-dicarbethoxy-2,6-dimethyl-1,4-dihydropyridine (I) as NADH model is reported.The N-acetyliminium intermediates are reduced in situ by I to give N-acetylamines (IV).Reduction of species which stabili
