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- W2953048284 abstract "Reductive cyclization of aryl and vinyl iodides tethered to vinylogous acyl triflates (VATs) induces a ring-expanding fragmentation to provide cyclic alkynyl ketones, including strained nine-membered cycloalkynes, in fair to excellent yield. The tandem cyclization/C-C bond-cleavage is initiated under carefully optimized conditions by halogen-metal exchange in the presence of carbonyl and vinyl triflate functionality. A modified protocol for alkylation of 1,3-cyclohexanedione is described for preparing the relevant VAT substrates." @default.
- W2953048284 created "2019-06-27" @default.
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- W2953048284 date "2011-05-19" @default.
- W2953048284 modified "2023-09-25" @default.
- W2953048284 title "ChemInform Abstract: Generation of Medium-Ring Cycloalkynes by Ring Expansion of Vinylogous Acyl Triflates." @default.
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- W2953048284 doi "https://doi.org/10.1002/chin.201124064" @default.
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