Catalytic Oxygenative Allylic Transposition of Alkenes into Enones with an Azaadamantane‐Type Oxoammonium Salt Catalyst. Issue 43 (12th July 2017)

• Record Type: Journal Article
• Authors: Nagasawa, Shota; Sasano, Yusuke; Iwabuchi, Yoshiharu
• Is Part Of: Chemistry. Volume 23:Issue 43(2017)
• Page Start: 10276
• Page End: 10279
• Publication Date: 2017-07-12
• Subjects: alkenes -- enones -- organocatalysis -- oxygenation -- synthetic methods; Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.201702512
• Languages: English
• ISSNs: 0947-6539

Abstract

Abstract: The first catalytic oxygenative allylic transposition of unactivated alkenes into enones has been developed using an oxoammonium salt as the catalyst. This reaction converts various tri‐ and trans ‐disubstituted alkenes into their corresponding enones with transposition of their double bonds at ambient temperature in good yields. The use of a less‐hindered azaadamantane‐type oxoammonium salt as the catalyst and a combination of two distinct stoichiometric oxidants, namely, iodobenzene diacetate and magnesium monoperoxyphthalate hexahydrate (MMPP⋅6 H2 O) are essential to facilitate the enone formation efficiently. Abstract : It takes two : The first catalytic oxygenative allylic transposition of unactivated alkenes into enones has been developed using an oxoammonium salt as the catalyst. This reaction converts various alkenes into their corresponding enones with transposition of their double bonds at ambient temperature in good yields. The use of a less‐hindered azaadamantane‐type oxoammonium salt as the catalyst and a combination of two distinct stoichiometric oxidants are essential.