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- W4249819273 endingPage "7341" @default.
- W4249819273 startingPage "7337" @default.
- W4249819273 abstract "Abstract Cyclopentadienes are valuable intermediates in organic synthesis and also ubiquitous as the Cp ligands in organometallic chemistry. As part of ongoing efforts to develop novel organic reactions that employ functionalized alkynes, a [3+2] cycloaddition of propargylic alcohols and ketene dithioacetals has been developed, which leads to fully substituted 2,5‐dialkylthio cyclopentadienes in good to excellent yields. In an unusual dethiolating Diels–Alder reaction, the cyclopentadienes were further reacted with maleimides to afford a family of novel fluorescent polycyclic compounds." @default.
- W4249819273 created "2022-05-12" @default.
- W4249819273 creator A5026672159 @default.
- W4249819273 creator A5031851632 @default.
- W4249819273 creator A5060496091 @default.
- W4249819273 creator A5066887020 @default.
- W4249819273 date "2014-05-30" @default.
- W4249819273 modified "2023-10-18" @default.
- W4249819273 title "[3+2] Cycloaddition of Propargylic Alcohols and α‐Oxo Ketene Dithioacetals: Synthesis of Functionalized Cyclopentadienes and Further Application in a Diels–Alder Reaction" @default.
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- W4249819273 doi "https://doi.org/10.1002/ange.201403014" @default.
- W4249819273 hasPublicationYear "2014" @default.
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