organic chemistry - Nitrobenzene reduction with (tin) Sn catalyst: Why is C-H bond cleavage preferred over O-H bond cleavage? - Chemistry Stack Exchange
organic chemistry - Pyridine synthesis by tin(II) chloride reduction of 5-nitronorbornene - Chemistry Stack Exchange
A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid - Yamabe - 2016 - Journal of Physical Organic Chemistry - Wiley Online Library
Bringing Out the Howitzers: Reactions of Aromatic Compounds - Functional Groups - Organic Chemistry I For Dummies, 2nd Edition (2014)
Tin(II) chloride
File:SnCl2 Nitro Reduction Scheme.svg - Wikimedia Commons
Facile synthesis of 2-substituted quinolines and 3-alkynyl-2-aryl-2 H -Indazole via SnCl 2 -mediated reductive cyclization - RSC Advances (RSC Publishing) DOI:10.1039/C4RA09153A
Proposal of a mechanism for the ester formation catalyzed by SnCl2/MxOy... | Download Scientific Diagram
What's the mechanism for the reduction of aromatic nitro group when using Fe and NH4Cl?
A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid - Yamabe - 2016 - Journal of Physical Organic Chemistry - Wiley Online Library
organic chemistry - Nitrobenzene reduction with (tin) Sn catalyst: Why is C-H bond cleavage preferred over O-H bond cleavage? - Chemistry Stack Exchange
A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid - Yamabe - 2016 - Journal of Physical Organic Chemistry - Wiley Online Library
Solved: Write the balanced equation for the reduction of 2,6-dimet... | Chegg.com
organic chemistry - Synthesis of Almotritpane - mechanism for educational purpose - Chemistry Stack Exchange
Stephen aldehyde synthesis - Wikipedia
Why do we use SnCl2 in the Stephen reaction? - Quora
Tin(II) chloride - Wikipedia
PVP-Pd nanoparticles as efficient catalyst for nitroarene reduction under mild conditions in aqueous media - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC02710E
![PDF] SnCl2/TiCl3-Mediated Deoximation of Oximes in an Aqueous Solvent | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f572c0db981382b43fc3efbbd7dbbe0c6b82b9e6/2-Table1-1.png "PDF] SnCl2/TiCl3-Mediated Deoximation of Oximes in an Aqueous Solvent | Semantic Scholar")
PDF] SnCl2/TiCl3-Mediated Deoximation of Oximes in an Aqueous Solvent | Semantic Scholar
A mechanism to understand. | Synthesis, Chemical, Understanding
Synthesis of 2,5-disubstitued benzimidazole using SnCl2-catalyzed reduction system at room temperature - ScienceDirect
Reduction of Nitro Groups, The Baeyer-Villiger, and Protection of Amines
Synthesis of 2,5-disubstitued benzimidazole using SnCl<sub>2</sub>-catalyzed reduction system at room temperature
