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- W2950131306 abstract "Abstract Allylsilanes serve as three-carbon dipole equivalents for the formation of tetrahydronaphthalenes via Lewis-acid promoted formal [3+3]-cycloadditions with benzylic cations. A competing [3+2]-pathway resulted in the formation of dihydro(1 H )indenes. Both quinone methides and benzylic alcohols were used as precursors to the benzylic cations." @default.
- W2950131306 created "2019-06-27" @default.
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- W2950131306 date "2010-08-18" @default.
- W2950131306 modified "2023-09-25" @default.
- W2950131306 title "ChemInform Abstract: Formal (3 + 3)- and (3 + 2)-Cycloadditions of Allylsilanes with Benzylic Cations." @default.
- W2950131306 cites W2019809260 @default.
- W2950131306 doi "https://doi.org/10.1002/chin.199504065" @default.
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