Efficient and continuous monoacylation with superior selectivity of symmetrical diamines in microreactors.
basic_science · Level V
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- Record sourced from PubMed, PMID 22030955.
- Also identified by DOI 10.1039/c1lc20765b.
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Abstract
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.