Metal-Free α-C(sp3)–H Functionalized Oxidative Cyclization of Tertiary N,N-Diaryl Amino Alcohols: Theoretical Approach for Mechanistic Pathway
The mechanistic pathway of TEMPO/I2-mediated oxidative cyclization of N,N-diaryl amino alcohols 1 was investigated. Based on direct empirical experiments, three key intermediates (aminium radical cation 3, α-aminoalkyl radical 4, and iminium 5), four types of reactive species (radical TEMPO, cationi...
Main Authors: | Zakir Ullah, Mihyun Kim |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2017-03-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/22/4/547 |
Similar Items
-
Vers la synthèse d'une nouvelle classe d'iminosucres conformationnellement contraints : ouverture d'azétidines, cyclisation 4-exo-trig et C-H amination catalytique
by: Nocquet, Pierre-Antoine
Published: (2013) -
Intramolecular C(sp3)–H Bond Amination Strategies for the Synthesis of Saturated N-containing Heterocycles
by: Jiayu Zhang, et al.
Published: (2020-11-01) -
An Acyl Radical Cascade Model for the Total Synthesis of Lyconadin A
by: Grant, Seth W.
Published: (2005) -
Eosin Y-catalyzed visible-light-mediated aerobic oxidative cyclization of N,N-dimethylanilines with maleimides
by: Zhongwei Liang, et al.
Published: (2015-04-01) -
Studies towards the synthesis of bioactive natural products and development of new synthetic methods
by: Khanizeman, Rabi'ah Nisha
Published: (2017)