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Volumn 5, Issue 18, 2007, Pages 2966-2974

Organocatalytic asymmetric destruction of 1-benzylated Reissert compounds catalysed by quaternary cinchona alkaloids

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST ACTIVITY; CATALYST SELECTIVITY; ENANTIOMERS; PHASE TRANSITIONS; REACTION KINETICS;

EID: 34548317441     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b710494d     Document Type: Article
Times cited : (19)

References (70)
  • 9
    • 0003780442 scopus 로고
    • C. Hansch, P. G. Sammes and J. B. Taylor, Pergamon Press, Oxford, 1st edn
    • Comprehensive Medicinal Chemistry, ed., C. Hansch, P. G. Sammes, and, J. B. Taylor, Pergamon Press, Oxford, 1st edn, 1990, vol. 3
    • (1990) Comprehensive Medicinal Chemistry, Ed.
  • 19
    • 0343463721 scopus 로고
    • For examples on racemic addition of electrophiles to Reissert compounds see:
    • A. Reissert Ber. Dtsch. Chem. Ges. 1905 38 3415
    • (1905) Ber. Dtsch. Chem. Ges. , vol.38 , pp. 3415
    • Reissert, A.1
  • 37
    • 33646855591 scopus 로고    scopus 로고
    • Alternative approaches to non-racemic 1-substituted Reissert compounds have previously been reported. For an enantioselective Reissert reaction involving 1-substituted isoquinolines see:
    • D. Brózda K. Hoffman M. D. Rozwadowska Heterocycles 2006 67 119
    • (2006) Heterocycles , vol.67 , pp. 119
    • Brózda, D.1    Hoffman, K.2    Rozwadowska, M.D.3
  • 39
    • 0037288295 scopus 로고    scopus 로고
    • Although only to a minor extent, decomposition of substrate 1 (R 1 = alkyl, Ar) to give 1-cyanoisoquinoline was also observed under the applied alkaline conditions and in the presence of air. See:
    • O. Sieck S. Schaller S. Grimme J. Liebscher Synlett 2003 337
    • (2003) Synlett , pp. 337
    • Sieck, O.1    Schaller, S.2    Grimme, S.3    Liebscher, J.4
  • 46
    • 0000308108 scopus 로고
    • E. L. Eliel and S. H. Wilen, Interscience, New York, p. 249. See also:
    • H. B. Kagan and J. C. Fiaud, in Topics in Stereochemistry, ed., E. L. Eliel, and, S. H. Wilen, Interscience, New York, 1988, vol. 18, p. 249. See also:
    • (1988) Topics in Stereochemistry, Ed.
    • Kagan, H.B.1    Fiaud In, J.C.2
  • 59
    • 33846597094 scopus 로고    scopus 로고
    • For kinetic resolutions involving quaternary cinchona alkaloids see:
    • H. Vogt S. Bräse Org. Biomol. Chem. 2007 5 406
    • (2007) Org. Biomol. Chem. , vol.5 , pp. 406
    • Vogt, H.1    Bräse, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.