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• W2055642657 abstract "Abstract The reaction of 4‐acetoxy‐2‐azetidinones with organoindium reagents generated in situ from indium and 1,4‐dibromo‐2‐butyne in the presence of LiCl in DMF selectively produced 2‐azetidinones which contain a 1,3‐butadienyl‐2‐yl group at the C4‐position in good yields. The Diels–Alder reaction of 4‐[(1‐methylene)prop‐2‐enyl]‐2‐azetidinones with a variety of dienophiles provided 2‐azetidinones with valuable functional‐group‐substituted six‐membered rings at the C4‐position in good yields." @default.
• W2055642657 created "2016-06-24" @default.
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• W2055642657 date "2007-10-18" @default.
• W2055642657 modified "2023-10-17" @default.
• W2055642657 title "Indium-Mediated Selective Introduction of a 1,3-Butadien-2-yl Group at the C4-Position in 2-Azetidinones and Application of 1,3-Diene-Tethered 2-Azetidinones in the Diels–Alder Reaction" @default.
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• W2055642657 doi "https://doi.org/10.1002/chem.200700796" @default.
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