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Cite the Following Article
Kinetics and mechanism of the anilinolysis of aryl phenyl isothiocyanophosphates in acetonitrile
Hasi Rani Barai and Hai Whang Lee
Beilstein J. Org. Chem. 2013, 9, 615–620.
https://doi.org/10.3762/bjoc.9.68
How to Cite
Barai, H. R.; Lee, H. W. Beilstein J. Org. Chem. 2013, 9, 615–620. doi:10.3762/bjoc.9.68
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Scholarly Works
- Barai, H. R.; Kim, J.-h.; Joo, S. W. Anilinolysis of O‐butyl phenyl phosphonochloridothioate in acetonitrile: Synthesis, characterization, kinetic study, and reaction mechanism. Journal of Physical Organic Chemistry 2017, 30, e3679. doi:10.1002/poc.3679
- Barai, H. R. Concerted Pathway to the Mechanism of the Anilinolysis of Bis(N,N-diethylamino)phosphinic Chloride in Acetonitrile. Australian Journal of Chemistry 2017, 70, 101–105. doi:10.1071/ch16202
- Barai, H. R.; Lee, H. W. Kinetics and Mechanism of Anilinolyses of Aryl Methyl and Aryl Propyl Chlorothiophosphates in Acetonitrile. Bulletin of the Korean Chemical Society 2014, 35, 2797–2802. doi:10.5012/bkcs.2014.35.9.2797
- Adhikary, K. K.; Lee, H. W. Significant Substituent Effects on Pyridinolysis of Aryl Ethyl Chlorophosphates in Acetonitrile. Bulletin of the Korean Chemical Society 2014, 35, 1460–1464. doi:10.5012/bkcs.2014.35.5.1460
- Barai, H. R.; Lee, H. W. Nucleophilic Substitution Reactions of O-Methyl N,N-Diisopropylamino Phosphonochloridothioate with Anilines and Pyridines. Bulletin of the Korean Chemical Society 2014, 35, 1016–1022. doi:10.5012/bkcs.2014.35.4.1016
- Barai, H. R.; Lee, H. W. Kinetics and Mechanism of Pyridinolyses of Aryl Methyl and Aryl Propyl Chlorothiophosphates in Acetonitrile. Bulletin of the Korean Chemical Society 2014, 35, 483–488. doi:10.5012/bkcs.2014.35.2.483
Patents
- FU MINGWEI; LI LINGCHAO; XIAO YA; GU WEN; MA YAN; GE MIN. REMDESIVIR-RELATED SUBSTANCE, AND PREPARATION METHOD THEREFOR AND USE THEREOF. WO 2022011727 A1, Jan 20, 2022.
