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Volumn 13, Issue 9, 2001, Pages 588-594

Chirality recognition in solvent-free solid-state crystallization: Chiral adduct formation by bis-β-naphthol derivatives and benzoquinone crystals

Author keywords

Benzoquinone; Bis naphthol derivatives; Charge transfer; Crystal to crystal transformation; Solid state crystallization; Solvent free conditions

Indexed keywords

BENZOQUINONE; HYDROGEN; NAPHTHALENE; NAPHTHOL DERIVATIVE; SOLVENT;

EID: 0034778792     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.1182     Document Type: Article
Times cited : (47)

References (12)
  • 1
    • 0347826811 scopus 로고
    • Solid state organic chemistry; efficient reactions, remarkable yields, and stereoselectivity
    • Toda F. Solid state organic chemistry; efficient reactions, remarkable yields, and stereoselectivity. Acc Chem Res 1995;28:480-486.
    • (1995) Acc Chem Res , vol.28 , pp. 480-486
    • Toda, F.1
  • 2
    • 0001614198 scopus 로고    scopus 로고
    • Formation of racemic compound crystals by mixing of two enantiomeric crystals in the solid state. Liquid transport of molecules from crystal to crystal
    • Toda F, Tanaka K, Miyamoto H, Koshima H, Miyahara I, Hirotsu K. Formation of racemic compound crystals by mixing of two enantiomeric crystals in the solid state. Liquid transport of molecules from crystal to crystal. J Chem Soc Perkin Trans 2 1997:1877-1885.
    • (1997) J Chem Soc Perkin Trans 2 , pp. 1877-1885
    • Toda, F.1    Tanaka, K.2    Miyamoto, H.3    Koshima, H.4    Miyahara, I.5    Hirotsu, K.6
  • 3
    • 0032538470 scopus 로고    scopus 로고
    • Stereoselective thermal conversion of s-trans-diallene into dimethylene cyclobutene via s-cis-diallene in the crystalline state
    • Toda F, Tanaka K, Tamashima T, Kato M. Stereoselective thermal conversion of s-trans-diallene into dimethylene cyclobutene via s-cis-diallene in the crystalline state. Angew Chem Int Ed 1998;37:2724-2727.
    • (1998) Angew Chem Int Ed , vol.37 , pp. 2724-2727
    • Toda, F.1    Tanaka, K.2    Tamashima, T.3    Kato, M.4
  • 4
    • 0003088016 scopus 로고    scopus 로고
    • Solid-state crystallization: Grinding together bis-β-naphthol and benzoquinone selectively generates only one of two adducts produced by solvent crystallization
    • Kuroda R, Imai Y, Tajima N, Sato T. Solid-state crystallization: grinding together bis-β-naphthol and benzoquinone selectively generates only one of two adducts produced by solvent crystallization. Proceedings of the Annual Conference of the Japanese Crystallographic Society 2000;83.
    • (2000) Proceedings of the Annual Conference of the Japanese Crystallographic Society , pp. 83
    • Kuroda, R.1    Imai, Y.2    Tajima, N.3    Sato, T.4
  • 5
    • 0001556541 scopus 로고    scopus 로고
    • Distribution of organic homomolecular crystals by chiral types and structural classes
    • Belsy VK, Zorkii PM. Distribution of organic homomolecular crystals by chiral types and structural classes. Acta Cryst 1997;33:1004-1006.
    • (1997) Acta Cryst , vol.33 , pp. 1004-1006
    • Belsy, V.K.1    Zorkii, P.M.2
  • 11
    • 0002123183 scopus 로고
    • A three-dimensional analysis of the crystal structure of p-benzoquinone
    • Trotter J. A three-dimensional analysis of the crystal structure of p-benzoquinone. Acta Cryst 1960;13:86-95.
    • (1960) Acta Cryst , vol.13 , pp. 86-95
    • Trotter, J.1
  • 12
    • 0001747277 scopus 로고
    • Refinement of the crystal structure of p-benzoquinone at -160°C
    • Bolhus F. van, Kiers, C. TH. Refinement of the crystal structure of p-benzoquinone at -160°C. Acta Cryst 1978;B34:1015-1016.
    • (1978) Acta Cryst , vol.B34 , pp. 1015-1016
    • Van Bolhus, F.1    Kiers, C.Th.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.