Woodward cis-hydroxylation
| Woodward cis-hydroxylation | |
|---|---|
| Named after | Robert Burns Woodward |
| Reaction type | addition reaction |
| Identifiers | |
| Organic Chemistry Portal | woodward-reaction |
The Woodward cis-hydroxylation (also known as the Woodward reaction) is the chemical reaction of alkenes with iodine and silver acetate in wet acetic acid to form cis-diols.[1][2](conversion of olefin into cis-diol)
The reaction is named after its discoverer, Robert Burns Woodward.
This reaction has found application in steroid synthesis.[3]
Reaction mechanism
The reaction of the iodine with the alkene is promoted by the silver acetate, thus forming an
anchimeric assistance, the iodine is displaced via another SN2 reaction to give an oxonium ion
(5), which is subsequently hydrolyzed to the give the mono-ester (6).
References
- ^ Woodward, R. B., U.S. patent 2,687,435
- ISSN 0002-7863.
- ISSN 0040-4039.