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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Regioselective double Kyodai nitration of toluene and chlorobenzene over zeolites. high preference for the 2,4-dinitro isomer at the second nitration stage.

[reaction: see text]. The Kyodai nitration of toluene and chlorobenzene has been examined in the presence of a solid inorganic catalyst (montmorillonite K10, zeolite HZSM-5, or HBEA-25). Regioselection was quite low at the mononitration stage, but a considerably high preference for the 2,4-isomer was observed at the dinitration stage.[1]

References

  1. Regioselective double Kyodai nitration of toluene and chlorobenzene over zeolites. high preference for the 2,4-dinitro isomer at the second nitration stage. Peng, X., Suzuki, H. Org. Lett. (2001) [Pubmed]
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