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- W2130553468 startingPage "713" @default.
- W2130553468 abstract "Abstract A synthetic method to stereoselectively prepare 4‐(cyclohexa‐1,3‐dienyl)‐1,3‐dioxolanes in good to excellent yields by gold(I)‐catalyzed [2+2+1] cycloaddition of 1,6‐diyne carbonates and esters with aldehydes is described. The cascade process involves 1,2‐acyloxy migration followed by cyclopropenation and cycloreversion. This leads to an unprecedented [2+2+1] cycloaddition of the resulting alkenylgold carbenoid species, examples of which are extremely rare, with two aldehyde molecules at catalyst loadings as low as 1 mol %. The usefulness of this cycloisomerization chemistry was further demonstrated by the transformation of one example to the corresponding phenol." @default.
- W2130553468 created "2016-06-24" @default.
- W2130553468 creator A5027691896 @default.
- W2130553468 creator A5039408031 @default.
- W2130553468 date "2013-12-09" @default.
- W2130553468 modified "2023-10-18" @default.
- W2130553468 title "Gold-Catalyzed [2+2+1] Cycloaddition of 1,6-Diyne Carbonates and Esters with Aldehydes to 4-(Cyclohexa-1,3-dienyl)-1,3-dioxolanes" @default.
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