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- W4282959361 abstract "We report an acid-catalyzed formal cycloaddition and dehydrative substitution reaction of tertiary propargylic alcohols and heteroareneboronic acids. The properties of the substituents on the alkynyl moiety determines the regioselectivity of the reaction, which could selectively construct fused heterocycles, tetrasubstituted allenes, or 1,3-dienes. This reaction proceeds efficiently with a wide array of substrate scope in up to 89% yield. A significant advantage of this protocol is the transition-metal-free and mild conditions needed." @default.
- W4282959361 created "2022-06-17" @default.
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- W4282959361 date "2022-06-16" @default.
- W4282959361 modified "2023-10-16" @default.
- W4282959361 title "Regioselective Cycloaddition and Substitution Reaction of Tertiary Propargylic Alcohols and Heteroareneboronic Acids via Acid Catalysis" @default.
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- W4282959361 doi "https://doi.org/10.1021/acs.orglett.2c01403" @default.
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