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Succinylsuccinate (or: succinylosuccinate) is a trivial name for esters of 2,5-dioxocyclohexane-1,4-dicarboxylic acid (or, in the more stable enol form: 1,4-dihydroxycyclohexa-1,4-diene dicarboxylic acids), obtained by the condensation of two molecules of succinic esters, compare: Nielsen, A. T.; Carpenter, W. R. Org. Synth. Coll. V; John Wiley & Sons: London, 1973, 288.
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Succinylsuccinate (or: succinylosuccinate) is a trivial name for esters of 2,5-dioxocyclohexane-1,4-dicarboxylic acid (or, in the more stable enol form: 1,4-dihydroxycyclohexa-1,4-diene dicarboxylic acids), obtained by the condensation of two molecules of succinic esters, compare: Nielsen, A. T.; Carpenter, W. R. Org. Synth. Coll. Vol. V; John Wiley & Sons: London, 1973, 288.
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2: (a) Herrmann, F. Justus Liebigs Ann. Chem. 1882, 211, 306.
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Compare: (c) Imai, M.; Ikuta, H.; Akahori, H.; Hasegawa, K.; Asano, M.; Tsujimoto, M. JP 57185237, 1982.
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Thermal transesterification of β-oxo esters (in the absence of a catalyst) is an old reaction: (a) Peters, T
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Thermal transesterification of β-oxo esters (in the absence of a catalyst) is an old reaction: (a) Peters, T. Justus Liebigs Ann. Chem. 1890, 257, 353.
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(a) Taber, D. F.; Amedio, J. C.; Patel, Y. K. J. Org. Chem. 1985, 50, 3618.
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39
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0037611582
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This pseudo-polymorphism is analogous to that described for the bromo analogue of 4b, for which X-ray crystal structures of both the solvent-free substance and a solvate are reported: Näther, C, Nagel, N, Bock, H, Seitz, W, Havlas, Z. Acta Crystallogr, Sect. B. 1996, 52, 697
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This pseudo-polymorphism is analogous to that described for the bromo analogue of 4b, for which X-ray crystal structures of both the solvent-free substance and a solvate are reported: Näther, C.; Nagel, N.; Bock, H.; Seitz, W.; Havlas, Z. Acta Crystallogr., Sect. B. 1996, 52, 697.
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