Three-Component Condensation of β-Ketonitriles, 4-Fluorobenzaldehyde, and Secondary Cyclic Amines
A new three-component condensation of β-ketonitriles, 4-fluorobenzaldehyde, and secondary cyclic amines was developed. A possible reaction mechanism has been proposed including Knoevenagel condensation followed by aromatic nucleophilic substitution. It was found that in the case of 3-oxopropanenitri...
Main Authors: | Dmitry V. Osipov, Kirill S. Korzhenko, Vitaly A. Osyanin |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-12-01
|
Series: | Reactions |
Subjects: | |
Online Access: | https://www.mdpi.com/2624-781X/3/4/42 |
Similar Items
-
A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
by: Daniel P. Pienaar, et al.
Published: (2019-12-01) -
Acylation of indolyl subsituted β-ketonitriles. The way to new indolo[2,3-c]pyrilium and β-carboline derivatives
by: N. M. Bogdan, et al.
Published: (2020-12-01) -
synthesis and characterization of modified MCM-41 and MCM-48 mesoporous and their application in Knoevenagel condensation reactions in water
by: Maryam Hajjami, et al.
Published: (2018-06-01) -
Microwave-Assisted Amination of a Chloropurine Derivative in the Synthesis of Acyclic Nucleoside Analogues
by: H.-G. Schmalz, et al.
Published: (2005-02-01) -
Leaving group ability in nucleophilic aromatic amination by sodium hydride-lithium iodide composite
by: Pang, Jia Hao, et al.
Published: (2022)