Journal
LAB ON A CHIP
Volume 12, Issue 1, Pages 65-68Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1lc20765b
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Efficient and continuous monoacylation of symmetrical diamines performed in microreactors yielded superior selectivity to that predicted by statistical considerations. It is highly valuable that the kinetically controlled product in high yields was achieved without any special catalyst at ambient temperature.
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