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- W2550360345 endingPage "5955" @default.
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- W2550360345 abstract "A variety of 3-aryl tetronic acids have been synthesized by an undirected, intermolecular C-H functionalization of arenes with 3-diazofuran-2,4-dione. This methodology featured as a key step in the synthesis of a series of naturally occurring 3-aryl-5-arylidene tetronic acids (pulvinates) from commercially available tetronic acid. Salient features of the pulvinic acid synthesis include a one-step, stereoselective synthesis of the C5 arylidene group and a single step introduction of the C3 aryl substituent." @default.
- W2550360345 created "2016-11-30" @default.
- W2550360345 creator A5050528304 @default.
- W2550360345 creator A5057253461 @default.
- W2550360345 date "2016-11-08" @default.
- W2550360345 modified "2023-09-25" @default.
- W2550360345 title "Catalytic Undirected Intermolecular C–H Functionalization of Arenes with 3-Diazofuran-2,4-dione: Synthesis of 3-Aryl Tetronic Acids, Vulpinic Acid, Pinastric Acid, and Methyl Isoxerocomate" @default.
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- W2550360345 doi "https://doi.org/10.1021/acs.orglett.6b03087" @default.
- W2550360345 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27934500" @default.
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