4.7 Article

First total synthesis of A2 isoprostane

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 67, Issue 12, Pages 4346-4351

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo025652f

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A stereoselective Julia-Lythgoe olefination has allowed the first total synthesis of A(2) isoprostane (1), a recently discovered member of the growing isoprostane family. This elusive compound opens up numerous new avenues for the molecular biology of cyclopentenone prostaglandins, which are endowed of intriguing biological effects such as antitumor, antiinflammatory, and antiviral activities.

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