Substrate dependent reaction channels of the Wolff–Kishner reduction reaction: A theoretical study
Wolff–Kishner reduction reactions were investigated by DFT calculations for the first time. B3LYP/6-311+G(d,p) SCRF=(PCM, solvent = 1,2-ethanediol) optimizations were carried out. To investigate the role of the base catalyst, the base-free reaction was examined by the use of acetone, hydrazine (H2N–...
Main Authors: | Shinichi Yamabe, Guixiang Zeng, Wei Guan, Shigeyoshi Sakaki |
---|---|
Format: | Article |
Language: | English |
Published: |
Beilstein-Institut
2014-01-01
|
Series: | Beilstein Journal of Organic Chemistry |
Subjects: | |
Online Access: | https://doi.org/10.3762/bjoc.10.21 |
Similar Items
-
Proton transfers in the Strecker reaction revealed by DFT calculations
by: Shinichi Yamabe, et al.
Published: (2014-08-01) -
An aniline dication-like transition state in the Bamberger rearrangement
by: Shinichi Yamabe, et al.
Published: (2013-06-01) -
Presence or absence of a novel charge-transfer complex in the base-catalyzed hydrolysis of N-ethylbenzamide or ethyl benzoate
by: Shinichi Yamabe, et al.
Published: (2013-01-01) -
Efficient Synthesis of Novel 1-Substituted β-Carboline Derivatives via Pictet-Spengler Cyclization of 5-Hydroxy-L-Tryptophan
by: Jani, N.A, et al.
Published: (2022) -
A new intermediate in the Prins reaction
by: Shinichi Yamabe, et al.
Published: (2013-03-01)