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- W2019302392 endingPage "3717" @default.
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- W2019302392 abstract "Treatment of the iridacyclopentadiene complex (1, R = CO2CH3) with silver tetrafluoroborate, followed by addition of a terminal alkyne (ethyne, ethyl ethnynyl ether, methyl propargyl ether), yields iridium(III) aryl-hydride complexes (6-H, R1 = H; 6-OEt, R1 = OCH2CH3; 6-CH2OMe, R1 = CH2OCH3). The structure of 6-OEt was established by X-ray crystallographic analysis. Treatment of 6-H with either HCl or carbon monoxide results in demetalation to give tetramethyl 1,2,3,4-benzenetetracarboxylate [C6(CO2Me)4H2]. When 3-butyn-2-ol and propargyl alcohol are employed as substrates, a similar reaction occurs with 1/AgBF4 to produce the phthalimidyl complexes (7-H, R1 = H; 7-Me, R1 = CH3). The lactone ring in 7 is generated from an intramolecular transesterification of the hydroxyl with an adjacent methyl ester. In all cases these products are attributed to tandem cycloaromatization and orthometalation processes." @default.
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- W2019302392 date "2001-07-17" @default.
- W2019302392 modified "2023-09-27" @default.
- W2019302392 title "Iridacyclopentadiene Reactions with Terminal Alkynes: Tandem Cycloaromatization and Orthometalation" @default.
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- W2019302392 doi "https://doi.org/10.1021/om0102450" @default.
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