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Volumn , Issue 14 SPEC. ISS., 2008, Pages 2303-2306

2,5-Dihydroxyterephthalates, 2,5-dichloro-1,4-benzoquinone-3,6- dicarboxylates, and polymorphic 2,5-dichloro-3,6-dihydroxyterephthalates

Author keywords

Arenes; Halogenation; Hydroquinones; Polymorphism; Quinones

Indexed keywords

ARSENIC COMPOUNDS; CHLORINE COMPOUNDS; SODIUM;

EID: 48549091907     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1067145     Document Type: Article
Times cited : (10)

References (39)
  • 1
    • 0042291889 scopus 로고    scopus 로고
    • Astruc, D, Ed, Wiley-VCH: Weinheim
    • (a) Modern Arene Chemistry; Astruc, D., Ed.; Wiley-VCH: Weinheim, 2002.
    • (2002) Modern Arene Chemistry
  • 3
    • 48549095920 scopus 로고    scopus 로고
    • 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.
    • 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.
  • 4
    • 84944868705 scopus 로고    scopus 로고
    • 2: (a) Herrmann, F. Justus Liebigs Ann. Chem. 1882, 211, 306.
    • 2: (a) Herrmann, F. Justus Liebigs Ann. Chem. 1882, 211, 306.
  • 6
    • 0343437668 scopus 로고    scopus 로고
    • 2: (c) Padias, A. B.; Hall, H. K. J. Org. Chem. 1985, 50, 5417.
    • 2: (c) Padias, A. B.; Hall, H. K. J. Org. Chem. 1985, 50, 5417.
  • 12
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    • US 3,124,582
    • (b) Jaffe, E. E. US 3,124,582, 1964.
    • (1964)
    • Jaffe, E.E.1
  • 13
    • 48549083930 scopus 로고    scopus 로고
    • Compare: (c) Imai, M.; Ikuta, H.; Akahori, H.; Hasegawa, K.; Asano, M.; Tsujimoto, M. JP 57185237, 1982.
    • Compare: (c) Imai, M.; Ikuta, H.; Akahori, H.; Hasegawa, K.; Asano, M.; Tsujimoto, M. JP 57185237, 1982.
  • 31
    • 48549102423 scopus 로고
    • Thermal transesterification of β-oxo esters (in the absence of a catalyst) is an old reaction: (a) Peters, T
    • 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.
    • (1890) Justus Liebigs Ann. Chem , vol.257 , pp. 353
  • 39
    • 0037611582 scopus 로고    scopus 로고
    • 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
    • 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.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.