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• W2950873747 startingPage "2449" @default.
• W2950873747 abstract "The reaction of aldehydes and ketones with an organoindium reagent generated in situ from indium and 1,6-dibromo-2,4-hexadiyne in the presence of lithium iodide in tetrahydrofuran (THF) selectively produced 1,6-diols linked to an allenyne unit with complete regioselectivity and chemoselectivity through 1,2-hexadien-4-yn-3,6-ylation, indicating that the organoindium acted as the 3,6-dianion reagent of 1,2-hexadien-4-yne." @default.
• W2950873747 created "2019-06-27" @default.
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• W2950873747 date "2007-11-05" @default.
• W2950873747 modified "2023-09-23" @default.
• W2950873747 title "Highly Selective Synthetic Method for 1,6-Diols Bearing Enyne Functions: Development of 3,6-Dianion Reagent of 1,2-Hexadien-4-yne Using 1,6-Dibromo-2,4-hexadiyne and Indium" @default.
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• W2950873747 doi "https://doi.org/10.1002/adsc.200700309" @default.
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