Site Selective Processes: A Combined Theoretical and Experimental Investigation of Thermally Activated Tautomerization Processes in 2(2,4-Dinitrobenzyl) Pyridine Derivatives
-
Add time:07/19/2019 Source:sciencedirect.com
The thermally activated NH→CH tautomerization process in crystals of 2(2,4-dinitrobenzyl) pyridine derivatives was investigated. The results indicate the absence of any trivial molecular structure–reactivity correlation, in contrast to what is found for similar systems in solutions. The absence of molecular structure–reactivity correlation in the crystalline state is attributed to the participation of neighboring molecules in the proton transfer process. A combined experimental and theoretical approach is presented and applied to the study of the tautomerization reaction in crystalline environments.
We also recommend Trading Suppliers and Manufacturers of 4-(2,4-DINITROBENZYL)PYRIDINE (cas 1603-85-6). Pls Click Website Link as below: cas 1603-85-6 suppliers
Prev:Tautomerism of 2-(2,4-dinitrobenzyl)pyridine
Next:Use of the 2,4-dinitrobenzyl protecting group in the synthesis of phosphorodithioate analogues of oligodeoxyribonucleotides) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Dealkylation of nucleoside arylmethyl 2-chlorophenyl phosphates: the 2,4-dinitrobenzyl protecting group07/20/2019
- Use of the 2,4-dinitrobenzyl protecting group in the synthesis of phosphorodithioate analogues of oligodeoxyribonucleotides07/21/2019
- Tautomerism of 2-(2,4-dinitrobenzyl)pyridine07/18/2019
- Photoinduced intramolecular proton transfer in 2- and 4-(2,4-dinitrobenzyl)pyridine07/17/2019


