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- W2056021915 abstract "Abstract While reaction of the bromoalkene with a 5-membered ketal 6a with tributyltin hydride gave only the acyclic product 18a , reaction of the corresponding bromoalkene with a 6-membered ketal 6b gave good yields of the cyclobutane 17b , in a novel ketal ring size effect. Also the gem -dicarboalkoxy effect was operative in these systems, e.g., cyclization of the bromo alkene triester 11a afforded reasonable yields of the cyclobutane 19 ." @default.
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- W2056021915 date "2010-08-02" @default.
- W2056021915 modified "2023-09-28" @default.
- W2056021915 title "ChemInform Abstract: gem-Disubstituent Effects in Small Ring Formation: Novel Ketal Ring Size Effect." @default.
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- W2056021915 doi "https://doi.org/10.1002/chin.199749090" @default.
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