A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid - Yamabe - 2016 - Journal of Physical Organic Chemistry - Wiley Online Library
File:SnCl2 Nitro Reduction Scheme.png - Wikimedia Commons
A DFT study of reduction of nitrobenzene to aniline with SnCl2 and hydrochloric acid - Yamabe - 2016 - Journal of Physical Organic Chemistry - Wiley Online Library
PVP-Pd nanoparticles as efficient catalyst for nitroarene reduction under mild conditions in aqueous media - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC02710E
File:SnCl2 Stephen reduction.svg - Wikimedia Commons
organic chemistry - Nitrobenzene reduction with (tin) Sn catalyst: Why is C-H bond cleavage preferred over O-H bond cleavage? - Chemistry Stack Exchange
Scheme 1. Reagents and conditions: (a) NaNO2, HCl, SnCl2, -5 ⁰C to RT,... | Download Scientific Diagram
Why do we use SnCl2 in the Stephen reaction? - Quora
Why do we use SnCl2 in the Stephen reaction? - Quora
RCN + SnCl2 + HCl → RCH = NH H2 +ORCHO This reaction is called Stephen reaction.
Solved Hi i am very confused with this please help by | Chegg.com
Tin(II) chloride
Synthesis of 2,5-disubstitued benzimidazole using SnCl2-catalyzed reduction system at room temperature - ScienceDirect
![The reaction RCN [ ]SnCl2/HCl (A) [ ]H2O RCHO + NH4Cl is known as:](https://d1hj4to4g9ba46.cloudfront.net/questions/1645507_1780626_ans_cfe45c9ca8fe42bd9c9eb464a1a38714.png "The reaction RCN [ ]SnCl2/HCl (A) [ ]H2O RCHO + NH4Cl is known as:")
The reaction RCN [ ]SnCl2/HCl (A) [ ]H2O RCHO + NH4Cl is known as:
organic chemistry - Selective reduction of nitro group to amine, in benzene ring containing nitrile? - Chemistry Stack Exchange
organic chemistry - Does this reduction mechanism of an diazonium via stannic chloride sense? - Chemistry Stack Exchange
Solved How do you complete the second step which is | Chegg.com
organic chemistry - Reaction mechanism for reduction of nitrobenzene to aniline in catalytic and acidic media - Chemistry Stack Exchange
Tin(II) chloride - Wikipedia
One-pot synthesis of 2,1-benzisoxazoles (anthranils) by a stannous chloride-mediated tandem reduction–heterocyclization of 2-nitroacylbenzenes under neutral conditions - ScienceDirect
What's the mechanism for the reduction of aromatic nitro group when using Fe and NH4Cl?
Reduction of Nitro Groups, The Baeyer-Villiger, and Protection of Amines
Stephen Reaction Mechanism, Stephen Aldehyde Synthesis Mechanism Explanation
Why do we use SnCl2 in the Stephen reaction? - Quora
