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Volumn 20, Issue 6, 2008, Pages 771-774

Pseudoasymmetry: A final twist?

Author keywords

Chirotopic; CIP; Hyoscyamine; Like unlike; Stereogenic; Trihydroxyglutaric acid

Indexed keywords

CYCLOBUTANE DERIVATIVE; CYCLOHEXANE DERIVATIVE; GLUTARIC ACID DERIVATIVE; ORGANIC COMPOUND;

EID: 45849153510     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20515     Document Type: Review
Times cited : (6)

References (9)
  • 1
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    • Stereochemistry of organic compounds. New York: Wiley
    • 667-668
    • Eliel EL, Wilen SH, Mander LN. Stereochemistry of organic compounds. New York: Wiley; 1994. p 67-69,667-668.
    • (1994) , pp. 67-69
    • Eliel, E.L.1    Wilen, S.H.2    Mander, L.N.3
  • 2
    • 0036154455 scopus 로고    scopus 로고
    • Stereochemical terminology and its discontents
    • Mislow K. Stereochemical terminology and its discontents. Chirality 2002;14:126-134.
    • (2002) Chirality , vol.14 , pp. 126-134
    • Mislow, K.1
  • 3
    • 8644262360 scopus 로고    scopus 로고
    • Pseudoasymmetry, stereogenicity, and the RS-nomenclature comprehended by the concepts of holantimers and stereoisograms
    • Fujita S. Pseudoasymmetry, stereogenicity, and the RS-nomenclature comprehended by the concepts of holantimers and stereoisograms. Tetrahedron 2004;60:11629-11638.
    • (2004) Tetrahedron , vol.60 , pp. 11629-11638
    • Fujita, S.1
  • 4
    • 0000993434 scopus 로고    scopus 로고
    • Prelog V, Helmchen G. Pseudoasymmetrie in der organischen Chemie. Helv Chim Acta 1972;55:2581-2598.
    • Prelog V, Helmchen G. Pseudoasymmetrie in der organischen Chemie. Helv Chim Acta 1972;55:2581-2598.
  • 5
    • 0009924476 scopus 로고
    • Stereoisomerism and local chirality
    • Mislow K, Siegel J. Stereoisomerism and local chirality. J Am Chem Soc 1984;106:3319-3328.
    • (1984) J Am Chem Soc , vol.106 , pp. 3319-3328
    • Mislow, K.1    Siegel, J.2
  • 9
    • 0020246368 scopus 로고
    • The unambiguous specification of the steric course of asymmetric syntheses
    • Seebach D, Prelog V. The unambiguous specification of the steric course of asymmetric syntheses. Angew Chem Int Ed Engl 1982;21:654-660.
    • (1982) Angew Chem Int Ed Engl , vol.21 , pp. 654-660
    • Seebach, D.1    Prelog, V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.