New Osmium-Based Reagent for the Dihydroxylation of Alkenes
Timothy J. Donohoe, Robert M. Harris, Sam Butterworth, Jeremy N. Burrows, A.R. Cowley, Jeremy S. Parker
Abstract
Timothy J. Donohoe, Robert M. Harris, Sam Butterworth, Jeremy N. Burrows, A.R. Cowley, Jeremy S. Parker
Abstract
The cis dihydroxylation of alkenes is most efficiently accomplished by reaction with osmium tetroxide. Recently, the expense and toxicity of osmium tetroxide have led to a number of attempts to harness alternative osmium-based reagents, including microencapsulation and solid support techniques. We describe here the development of a new nonvolatile, stable, and recoverable osmium-based reagent devised for the stoichiometric cis dihydroxylation of alkenes. Although attempts to make this new dihydroxylation work with catalytic amounts of this reagent were unsuccessful, we did develop a sensitive test for free osmium tetroxide leached from the reagent in situ: this test may well have uses in probing future applications of derivatized osmium reagents.
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The cis dihydroxylation of alkenes is most efficiently accomplished by reaction with osmium tetroxide. Recently, the expense and toxicity of osmium tetroxide have led to a number of attempts to harness alternative osmium-based reagents, including microencapsulation and solid support techniques. We describe here the development of a new nonvolatile, stable, and recoverable osmium-based reagent devised for the stoichiometric cis dihydroxylation of alkenes. Although attempts to make this new dihydroxylation work with catalytic amounts of this reagent were unsuccessful, we did develop a sensitive test for free osmium tetroxide leached from the reagent in situ: this test may well have uses in probing future applications of derivatized osmium reagents.
Key concepts: Dihydroxylation, Osmium, Osmium tetroxide, Reagent, Chemistry, Stoichiometry, Combinatorial chemistry, Organic chemistry