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Volumn 3, Issue 19, 2001, Pages 2985-2987

Asymmetric synthesis of (-)-indolizidine 209D via B-alkyl Suzuki coupling and amination reactions

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; AMINE; INDOLIZIDINE 209D; INDOLIZINE DERIVATIVE; NICOTINIC RECEPTOR BLOCKING AGENT;

EID: 0035922319     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0163171     Document Type: Article
Times cited : (52)

References (50)
  • 3
    • 0020336489 scopus 로고
    • Their structures have been tentatively assigned on the basis of the mass spectrum [Daley, J. W. Fortschr. Chem. Org. Naturst. 1982, 41, 205].
    • (1982) Fortschr. Chem. Org. Naturst. , vol.41 , pp. 205
    • Daley, J.W.1
  • 23
    • 0346786657 scopus 로고    scopus 로고
    • (b) Suzuki, A. J. Organomet. Chem. 1999, 576, 147. For recent application (b) natural product syntheses, see:
    • (1999) J. Organomet. Chem. , vol.576 , pp. 147
    • Suzuki, A.1
  • 45
    • 0042294778 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, Chapter 27
    • (a) Yanagisawa, A. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999; Chapter 27.
    • (1999) Comprehensive Asymmetric Catalysis
    • Yanagisawa, A.1
  • 46
    • 0035804479 scopus 로고    scopus 로고
    • and references therein
    • (b) Kii, S.; Maruoka, K. Tetrahedron Lett. 2001, 42, 1935 and references therein.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 1935
    • Kii, S.1    Maruoka, K.2
  • 49
    • 0041793616 scopus 로고    scopus 로고
    • note
    • Otherwise, an increasing amount of byproducts was formed, presumably by reaction with MeOH under these conditions. However, after separation, the product was relatively stable in MeOH solution even at room temperature.
  • 50
    • 0041292959 scopus 로고    scopus 로고
    • note
    • The formation of diastereomer 2 was not observed by NMR.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.