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- W2022181260 abstract "Ozonolysis of 1 largely results in 2 and 3, having features similar to several classes of natural products. The retention of the C15 pericycle suggests preference for the cleavage of π-bonds endo to the cyclopentane ring. This unique property of trindane offers opportunities for synthesis of complex natural products from this hydrocarbon that can be made in quantity by acid-catalyzed trimerizatiion of cyclopentanone." @default.
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- W2022181260 date "2001-07-14" @default.
- W2022181260 modified "2023-10-18" @default.
- W2022181260 title "One-Step Transformation of Tricyclopentabenzene (Trindane, C<sub>15</sub>H<sub>18</sub>) to Bicyclo(10.3.0)pentadec-1(12)ene- 2,6,7,11-tetrone (C<sub>15</sub>H<sub>18</sub>O<sub>4</sub>) and Its Aldol Product, 12-Hydroxy-16-oxatetracyclo(10.3.1.0.<sup>1,5</sup>0<sup>7,11</sup>)hexadec-7(11)ene-2,6-dione (C<sub>15</sub>H<sub>18</sub>O<sub>4</sub>)" @default.
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- W2022181260 doi "https://doi.org/10.1021/ol010086g" @default.
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