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Volumn 2010, Issue 3, 2010, Pages 45-55

A DITOX derived α-sulfinyl carbanion as nucleophile in conjugate addition reactions to pyrrolo[2,1-a]isoquinolones

Author keywords

sulfinyl carbanion; Asymmetric oxidation; Conjugate addition; DITOX; Pyrroloisoquinolines

Indexed keywords


EID: 77953367295     PISSN: 15517012     EISSN: 15517004     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (63)
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    • (d) Yamamguchi, M. In Comprehensive Asymmetric Catalysis I-III, Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H. Eds.; Springer: Berlin, 1999, Vol. 3, pp 1121.
    • (1999) Comprehensive Asymmetric Catalysis I-III , vol.3 , pp. 1121
    • Yamamguchi, M.1
  • 7
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    • (f) Iguchi, M.; Yamada, K.; Tomioka, K. In Organolithiums in Enantioselective Synthesis, Hodgson, D. M., Ed.; Topics in Organometallic Chemistry, Springer: Berlin, 2003, Vol. 5, pp 21-36.
    • (2003) Organolithiums in Enantioselective Synthesis , vol.5 , pp. 21-36
    • Iguchi, M.1    Yamada, K.2    Tomioka, K.3
  • 13
    • 77953365127 scopus 로고    scopus 로고
    • For reviews on asymmetric conjugate additions with sulfoxide stabilized carbanions, see
    • For reviews on asymmetric conjugate additions with sulfoxide stabilized carbanions, see:
  • 14
    • 0000231514 scopus 로고
    • In, Morrison, J. D., Ed.; Academic Press: New York
    • (a) Solladié, G. In Asymmetric Synthesis; Morrison, J. D., Ed.; Academic Press: New York, 1983; Vol. 2, pp 157.
    • (1983) Asymmetric Synthesis , vol.2 , pp. 157
    • Solladié, G.1
  • 15
    • 0002335594 scopus 로고
    • In, Patai, S., Rappoport, Z., Striling, C. J. M., Eds.; Wiley-Interscience: New York
    • (b) Posner, G. H. In The Chemistry of Sulfones and Sulfoxides; Patai, S., Rappoport, Z., Striling, C. J. M., Eds.; Wiley-Interscience: New York, 1988; pp 823-849.
    • (1988) The Chemistry of Sulfones and Sulfoxides , pp. 823-849
    • Posner, G.H.1
  • 37
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    • For some representative examples, see: reductions
    • For some representative examples, see: reductions
  • 47
    • 77953419289 scopus 로고    scopus 로고
    • For examples of low reactivity of α, β-unsaturated amides and lactams in 1, 4-addition reactions, see
    • For examples of low reactivity of α, β-unsaturated amides and lactams in 1, 4-addition reactions, see:
  • 48
    • 3042780198 scopus 로고    scopus 로고
    • and references therein. For examples for 1, 4-addition reactions of sulfur-stabilized anions to lactams, see
    • (a) Brewster, A. G.; Broady, S.; Hughes, M.; Moloney, M. G.; Woods, G. Org. Biomol. Chem. 2004, 2, 1800, and references therein. For examples for 1, 4-addition reactions of sulfur-stabilized anions to lactams, see:
    • (2004) Org. Biomol. Chem. , vol.2 , pp. 1800
    • Brewster, A.G.1    Broady, S.2    Hughes, M.3    Moloney, M.G.4    Woods, G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.