Organic peroxide in the context of "1,2,4-trioxane"

The hydroxyl radical, denoted as •OH or HO•, is the neutral form of the hydroxide ion (OH). As a free radical, it is highly reactive and consequently short-lived, making it a pivotal species in radical chemistry.

In nature, hydroxyl radicals are most notably produced from the decomposition of hydroperoxides (ROOH) or, in atmospheric chemistry, by the reaction of excited atomic oxygen with water. They are also significant in radiation chemistry, where their formation can lead to hydrogen peroxide and oxygen, which in turn can accelerate corrosion and stress corrosion cracking in environments such as nuclear reactor coolant systems. Other important formation pathways include the UV-light dissociation of hydrogen peroxide (H₂O₂) and the Fenton reaction, where trace amounts of reduced transition metals catalyze the breakdown of peroxide.

Artemisinin (/ˌɑːrtɪˈmiːsɪnɪn/) and its semisynthetic derivatives are a group of drugs used in the treatment of malaria due to Plasmodium falciparum. It was discovered in 1972 by Tu Youyou, who shared the 2015 Nobel Prize in Physiology or Medicine for her discovery. Artemisinin-based combination therapies (ACTs) have become standard treatment worldwide for P. falciparum malaria as well as malaria due to other species of Plasmodium. Artemisinin can be extracted from the herb Artemisia annua (sweet wormwood), which is used in traditional Chinese medicine. Alternatively, it can be prepared by a semi-synthetic method from a precursor compound that can be produced using a genetically engineered yeast, which is much more efficient than extraction from the plant.

Artemisinin and its derivatives are all sesquiterpene lactones containing an unusual peroxide bridge. This endoperoxide 1,2,4-trioxane ring is responsible for their antimalarial properties. Few other natural compounds with such a peroxide bridge are known.