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Efficient One-Pot Synthesis of Indolhydroxy Derivatives Catalyzed by SnCl2, DFT Calculations and Docking Study | Chemistry Africa
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organic chemistry - Pyridine synthesis by tin(II) chloride reduction of 5-nitronorbornene - Chemistry Stack Exchange
Studies on the Reduction of the Nitro Group in 4-Nitroindazoles by Anhydrous SnCl<sub>2</sub> in Different Alcohols
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Synthesis of 2,5-disubstitued benzimidazole using SnCl2-catalyzed reduction system at room temperature - ScienceDirect
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organic chemistry - How to do work up of reactions (Problem of Emulsion) where NO2 group is reduced using SnCl2.2H2O? - Chemistry Stack Exchange
Reductive Aromatization/Dearomatization and Elimination Reactions to Access Conjugated Polycyclic Hydrocarbons, Heteroacenes, an
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organic chemistry - Selective reduction of nitro group to amine, in benzene ring containing nitrile? - Chemistry Stack Exchange
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A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid - Yamabe - 2016 - Journal of Physical Organic Chemistry - Wiley Online Library
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One-pot synthesis of 2,1-benzisoxazoles (anthranils) by a stannous chloride-mediated tandem reduction–heterocyclization of 2-nitroacylbenzenes under neutral conditions - ScienceDirect
![SOLVED: The first step in the synthesis of lidocaine is a reduction reaction. Which compound serves as the reducing reagent in this reaction? SnCl2, HCl, or KOH? SOLVED: The first step in the synthesis of lidocaine is a reduction reaction. Which compound serves as the reducing reagent in this reaction? SnCl2, HCl, or KOH?](https://cdn.numerade.com/ask_images/f0ece05402c54da88da163a8a9259443.jpg)
SOLVED: The first step in the synthesis of lidocaine is a reduction reaction. Which compound serves as the reducing reagent in this reaction? SnCl2, HCl, or KOH?
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