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- W2004169884 abstract "Abstract Several new 4‐thio‐4,5‐dihydro‐2(3 H )‐furanones were prepared by the conjugate addition reactions of different thioacids, dithioacids, xanthates and dithiocarbamates to 2(5 H )‐furanones. When 5‐methyl‐2(5 H )‐furanone was used as the electrophilic substrate, the reaction was diastereoselective affording exclusively the cis ‐α,β‐disubstituted butanolides. Some adducts were selectively hydrolysed to deliver a free thiol functionality. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)" @default.
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- W2004169884 date "2004-03-18" @default.
- W2004169884 modified "2023-10-17" @default.
- W2004169884 title "A Study of the Conjugate Addition of Thionucleophiles to 2(5<i>H</i>)‐Furanones" @default.
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- W2004169884 doi "https://doi.org/10.1002/ejoc.200300693" @default.
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