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Metal-Free C–H Difluoromethylation of Imidazoles with the R..:
Denys A. Kvasha (14266435)
;
Andrii Deviatkin (14266438)
;
Andrii S. Poturai (14266441)
...
https://figshare.com/articles/journal_contribution/Metal-Free_C_H_Difluoromethylation_of_Imidazoles_with_the_Ruppert_Prakash_Reagent/21737041. , 2022
Link:
https://doi.org/10.1021/acs.joc.2c02041.s001
RT Journal T1
Metal-Free C–H Difluoromethylation of Imidazoles with the Ruppert–Prakash Reagent
UL https://suche.suub.uni-bremen.de/peid=base-ftunivfreestate:oai:figshare.com:article_21737041&Exemplar=1&LAN=DE A1 Denys A. Kvasha (14266435) A1 Andrii Deviatkin (14266438) A1 Andrii S. Poturai (14266441) A1 Pavel S. Nosik (6631394) A1 Andrii A. Kyrylchuk (11831833) A1 Sergiy Suikov (14266444) A1 Alexander B. Rozhenko (1676053) A1 Dmitriy M. Volochnyuk (1617088) A1 Oleksandr O. Grygorenko (1617082) YR 2022 K1 Biophysics K1 Biochemistry K1 Medicine K1 Molecular Biology K1 Evolutionary Biology K1 Developmental Biology K1 Infectious Diseases K1 Computational Biology K1 Biological Sciences not elsewhere classified K1 Chemical Sciences not elsewhere classified K1 Physical Sciences not elsewhere classified K1 Information Systems not elsewhere classified K1 quantum chemical calculations K1 >- difluoromethylation ) K1 high activation barriers K1 first proposed mechanism K1 2 -( trimethylsilyl K1 imidazoles gives products K1 formal difluorocarbene insertion K1 2 </ sub K1 3 </ sub K1 proposed mechanisms K1 activation barrier K1 2 position K1 2 atom K1 c </ K1 substituted imidazoles K1 substituted imidazole K1 substituted derivatives K1 solvent molecules K1 slowly convert K1 nmr spectra K1 include steps K1 e K1 difluorocarbene without K1 carbon atom K1 barrierless addition K1 adduct attacks K1 3 atom JF https://figshare.com/articles/journal_contribution/Metal-Free_C_H_Difluoromethylation_of_Imidazoles_with_the_Ruppert_Prakash_Reagent/21737041 LK http://dx.doi.org/https://doi.org/10.1021/acs.joc.2c02041.s001 DO https://doi.org/10.1021/acs.joc.2c02041.s001 SF ELIB - SuUB Bremen
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