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Abstract
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Various cis- and trans-aziridine derivatives were deaminated via the reaction with task-specific silica immobilized organosilane-
based nitrite ionic liquid. Corresponding cis- or trans-alkenes were produced as stereospecific products in goodto-
excellent yields. The advantages of this method include the one-pot procedure, operational simplicity, solvent-free, and
very short reaction times. Simple handling of this nitrite anion source nanoparticles and thus lowering the risks and hazards
of a chemical process can offer other important advantages.
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