1988
DOI: 10.1016/s0040-4039(00)80169-0
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Selective reduction of aromatic / aliphatic nitro groups by sodium sulfide.

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Cited by 43 publications
(8 citation statements)
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“…Due to H2S reducing properties it can reduce azide and nitro groups [14,15] [43] and this is used for H2S detection using different fluorescent probes (Figure 3) [44][45][46].…”
Section: Chemical Reduction Methodsmentioning
confidence: 99%
“…Due to H2S reducing properties it can reduce azide and nitro groups [14,15] [43] and this is used for H2S detection using different fluorescent probes (Figure 3) [44][45][46].…”
Section: Chemical Reduction Methodsmentioning
confidence: 99%
“…This has so far only been described using stoichiometric amounts of Na 2 S in moderate yields of 70%. 83 Recycling experiments…”
Section: View Article Onlinementioning
confidence: 99%
“…Often released from benzothiazole derivatives by hydrolysis, the source is atom inefficient, and the removal of the C2 carbon requires a lot of energy, so there is an opportunity for improvement [62,63]. An alternative legacy method is using the Zinin reduction of 2-nitrochlorobenzene [64][65][66][67], although the reported yields for this process are generally modest at best, and there appears to have been little investigation into this process in recent times. While the formation of the ring-opened aminothiophenol from the benzodithiazole (Scheme 21) is also incredibly simple, it is also the limitations of average yields and product contamination with, e.g., sulphur residues that are problematic.…”
Section: Synthesis Of Aminothiophenolsmentioning
confidence: 99%