The modification of the Prévost reaction to form cis-glycols by the treatment of olefins with iodine and silver acetate in wet acetic acid is generally known as the Woodward cis-hydroxylation. This reaction is usually carried out in two steps and has been compared with Woodward cis-hydroxylation. A more competitive reaction, the Sharpless dihydroxylation, has also been explored since it also produces cis-glycols. The Prévost reaction has limited applications in organic synthesis
CITATION STYLE
Waldvogel, S. R. (2010). Comprehensive Organic Name Reactions and Reagents. Synthesis, 2010(05), 892–892. https://doi.org/10.1055/s-0029-1218680
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