Abstract
Under mild conditions and without the use of toxic metals, the oxidation of primary alcohols and aldehydes to the corresponding carboxylic acids with 1-hydroxy-1,2-benziodoxole-3(1H)-one-1-oxide (IBX) proceeds in the presence of 1-hydroxypyridine or N-hydroxysuccinimide (see scheme). The reaction tolerates a wide variety of functional groups.
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Mazitschek, R., M̈lbaier, M., & Giannis, A. (2002). IBX-mediated oxidation of primary alcohols and aldehydes to form carboxylic acids. Angewandte Chemie - International Edition, 41(21), 4059–4061. https://doi.org/10.1002/1521-3773(20021104)41:21<4059::AID-ANIE4059>3.0.CO;2-R
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