Milas hydroxylation

The Milas hydroxylation is an organic reaction converting an alkene to a vicinal diol, and was developed by Nicholas A. Milas in the 1930s. The cis-diol is formed by reaction of alkenes with hydrogen peroxide and either ultraviolet light or a catalytic osmium tetroxide, vanadium pentoxide, or chromium trioxide.

Source: Wikipedia — Milas hydroxylation (CC BY-SA 4.0)

Milas hydroxylation

The Milas hydroxylation is an organic reaction converting an alkene to a vicinal diol, and was developed by Nicholas A. Milas in the 1930s. The cis-diol is formed by reaction of alkenes with hydrogen peroxide and either ultraviolet light or a catalytic osmium tetroxide, vanadium pentoxide, or chromium trioxide.

This neuron ends here.

Source: Wikipedia "Milas hydroxylation" · CC BY-SA 4.0

Share this article: X · Bluesky
Privacy Policy