Substrate dependent reaction channels of the Wolff–Kishner reduction reaction: A theoretical study

Shinichi Yamabe, Guixiang Zeng, Wei Guan and Shigeyoshi Sakaki
Beilstein J. Org. Chem. 2014, 10, 259–270. https://doi.org/10.3762/bjoc.10.21

Supporting Information

Supporting Information File 1: Full citation of reference [46], Figure S1 for the neutral reaction, and Cartesian coordinates of optimized geometries in Figure 1, Figure 3, Figure 5 and Figure 6.
Format: PDF Size: 565.2 KB Download

Cite the Following Article

Substrate dependent reaction channels of the Wolff–Kishner reduction reaction: A theoretical study
Shinichi Yamabe, Guixiang Zeng, Wei Guan and Shigeyoshi Sakaki
Beilstein J. Org. Chem. 2014, 10, 259–270. https://doi.org/10.3762/bjoc.10.21

How to Cite

Yamabe, S.; Zeng, G.; Guan, W.; Sakaki, S. Beilstein J. Org. Chem. 2014, 10, 259–270. doi:10.3762/bjoc.10.21

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Düfert, A. Oxidation und Reduktion. Organische Synthesemethoden; Springer Berlin Heidelberg, 2023; pp 333–479. doi:10.1007/978-3-662-65244-2_4
  • Gnatovsky, G. R.; Orel, V. B.; Vitkovskaya, N. M. The addition of ethylhydrazine to α,β- and β,γ-unsaturated ketones: a quantum-chemical modeling. Journal of Physics: Conference Series 2021, 1847, 012052. doi:10.1088/1742-6596/1847/1/012052
  • doi:10.1002/9783527828166.ch8
  • Zhou, X.-Y.; Chen, X. Recyclable Pd/C catalyzed one-step reduction of carbonyls to hydrocarbons under simple conditions without extra base. Tetrahedron Letters 2020, 61, 151447. doi:10.1016/j.tetlet.2019.151447
  • Xia, Z.; Zheng, C.; Liang, X.; Cai, Y.; You, S. Manipulation of Spiroindolenine Intermediates for Enantioselective Synthesis of 3‐(Indol‐3‐yl)‐Pyrrolidines. Angewandte Chemie 2018, 131, 1170–1174. doi:10.1002/ange.201812344
  • Xia, Z.-L.; Zheng, C.; Liang, X.-W.; Cai, Y.; You, S.-L. Manipulation of Spiroindolenine Intermediates for Enantioselective Synthesis of 3-(Indol-3-yl)-Pyrrolidines. Angewandte Chemie (International ed. in English) 2018, 58, 1158–1162. doi:10.1002/anie.201812344
  • Murray, B. A. doi:10.1002/9781118941829.ch1
  • Banerji, K. K. doi:10.1002/9781118941829.ch3
  • Xu, R.-Q.; Gu, Q.; You, S.-L. Construction of the Benzomesembrine Skeleton: Palladium(0)-Catalyzed Intermolecular Arylative Dearomatization of α-Naphthols and Subsequent Aza-Michael Reaction. Angewandte Chemie (International ed. in English) 2017, 56, 7252–7256. doi:10.1002/anie.201703674
  • Xu, R.; Gu, Q.; You, S. Construction of the Benzomesembrine Skeleton: Palladium(0)‐Catalyzed Intermolecular Arylative Dearomatization of α‐Naphthols and Subsequent Aza‐Michael Reaction. Angewandte Chemie 2017, 129, 7358–7362. doi:10.1002/ange.201703674
  • Banerji, K. K. Organic Reaction Mechanisms Series; Wiley, 2015; pp 91–170. doi:10.1002/9781118930786.ch3
Other Beilstein-Institut Open Science Activities