Английская Википедия:1,3,4-Oxadiazole

Материал из Онлайн справочника
Версия от 02:36, 18 декабря 2023; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Chembox <!-- Images --> | ImageFile = 1,3,4-oxadiazole.svg | ImageSize = 120px <!-- Names --> | PIN = 1,3,4-Oxadiazole | OtherNames = <!-- Sections --> | Section1 = {{Chembox Identifiers | CASNo = 288-99-3 | PubChem = 97428 | ChemSpiderID = 87937 | UNII = 20O2F20OUR | SMILES = C1=NN=CO1 | StdInChI=1S/C2H2N2O/c1-3-4-2-5-1/h1-2H | StdInChIKey = FKASFBLJDCHBNZ-UHFFFAOYSA-N }} | Secti...»)
(разн.) ← Предыдущая версия | Текущая версия (разн.) | Следующая версия → (разн.)
Перейти к навигацииПерейти к поиску

Шаблон:Chembox

1,3,4-Oxadiazole is a nitrogen and oxygen containing heterocycle, and one of the four isomers of oxadiazole.[1][2]

Derivatives

1,3,4-Oxadiazole itself is not commonly used in organic chemistry, but many of its derivatives are important. For example, raltegravir is an HIV drug which contains an 1,3,4-oxadiazole ring. Other pharmaceutical drugs containing the 1,3,4-oxadiazole ring include fenadiazole, zibotentan, and tiodazosin.

1,3,4-Oxadiazole derivatives can be synthesized in a variety of ways.[3] One pathway is from oxidation of tetrazoles in the presence of aldehydes.[4] Similarly, the reaction of tetrazoles with acyl chlorides provides oxadiazoles.[5] Both methods involve the release of N2.

See also

References