1361875-59-3Relevant academic research and scientific papers
Ruthenium-Catalyzed Reductive Amidation without an External Hydrogen Source
Yagafarov, Niyaz Z.,Muratov, Karim M.,Biriukov, Klim,Usanov, Dmitry L.,Chusova, Olga,Perekalin, Dmitry S.,Chusov, Denis
, p. 557 - 563 (2018)
A catalytic reaction between aldehydes and primary amides that leads to N-alkylated amides was investigated. The developed protocol employs carbon monoxide as a deoxygenative agent and, therefore, avoids the use of an external hydrogen source. Cyclopentad
One-pot stibine modified Co2(CO)8 catalyzed reductive N-alkylation of primary amides with carbonyl compounds
Rubio-Pérez, Laura,Sharma, Pankaj,Pérez-Flores, F. Javier,Velasco, Luis,Arias, J. Luis.,Cabrera, Armando
experimental part, p. 2342 - 2348 (2012/04/10)
A one-pot stibine modified Co2(CO)8 homogeneous catalytic reductive N-alkylation of primary amides using aldehydes/ketones as alkylating agents, is reported. Good to excellent yields of a wide range of secondary amides are obtained (up to 97%) under relative mild conditions.
