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Ruđer Bošković Institute, Bijenička cesta 54, HR-10002 Zagreb, Croatia
E-mail: mmaksic@emma.irb.hr
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McGill University, Department of Chemistry and FQRNT Centre for Green Chemistry and Catalysis, 801 Sherbrooke St., H3A 0B8 Montréal, Canada
E-mail: tomislav.friscic@mcgill.ca
Chem. Commun., 2012,48, 9705-9707
DOI:
10.1039/C2CC34013E
Received
05 Jun 2012,
Accepted
13 Aug 2012
First published online
13 Aug 2012
ortho- and para-Phenylenediamines were desymmetrised and quantitatively transformed into mono- and bis-(thio)ureas or mixed thiourea–ureas through a one-pot mechanochemical click reaction sequence; mechanochemical desymmetrisation proceeds quantitatively without excess reagents and allows the controlled extension of a molecular structure by combining normally competing reactions.
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