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- W2276999119 endingPage "2069" @default.
- W2276999119 startingPage "2062" @default.
- W2276999119 abstract "An efficient, environmentally friendly and one-pot route to new 9-aryl/9-arylethynyl-2,3,4,9-tetrahydro-1H-xanthen-1-one derivatives from inexpensive starting materials has been developed. This method proceeded by a domino nucleophilic-substitution/intramolecular cyclization/dehydration sequence of propargylic amines/diaryl amines and 1,3-cyclohexanediones under the promotion of FeCl3, which involved the formation of two new σ (C-C and C-O) bonds in a single operation for the construction of novel tetrahydroxanthene skeletons in 68-95% yields." @default.
- W2276999119 created "2016-06-24" @default.
- W2276999119 creator A5016411880 @default.
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- W2276999119 creator A5091562588 @default.
- W2276999119 date "2016-02-22" @default.
- W2276999119 modified "2023-10-18" @default.
- W2276999119 title "FeCl<sub>3</sub>-Mediated One-Pot Domino Reactions for the Synthesis of 9-Aryl/9-Arylethynyl-2,3,4,9-tetrahydro-1<i>H</i>-xanthen-1-ones from Propargylic Amines/Diaryl Amines and 1,3-Cyclohexanediones" @default.
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- W2276999119 doi "https://doi.org/10.1021/acs.joc.6b00001" @default.
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