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Volumn 15, Issue 10, 2004, Pages 1164-1166

A concise total synthesis of S-(+)-tylophorine

Author keywords

Biological activity; Phenanthroindolizidine alkaloid; Tylophorine

Indexed keywords

TYLOPHORINE;

EID: 7244255724     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (31)

References (10)
  • 2
    • 0035210509 scopus 로고    scopus 로고
    • For recent reviews, see: Z. Li, Z. Jin, R. Huang, Synthesis, 2001, 2365. For recent synthesis of tylophorine also see: (a) D. L. Comins, L. A. Morgan, Tetrahedron Lett., 1991, 32, 5919. (b) W. H. Pearson, R. Walavalkar, Tetrahedron Lett., 1994, 50, 12293. (c) M. A. Ciufolini, F. Roschangar, J. Am. Chem. Soc., 1996, 118, 12082. (d) D. L. Comins, X. Chen, L. A. Morgan, J. Org. Chem., 1997, 62, 7435.
    • (2001) Synthesis , pp. 2365
    • Li, Z.1    Jin, Z.2    Huang, R.3
  • 3
    • 0026044470 scopus 로고
    • For recent reviews, see: Z. Li, Z. Jin, R. Huang, Synthesis, 2001, 2365. For recent synthesis of tylophorine also see: (a) D. L. Comins, L. A. Morgan, Tetrahedron Lett., 1991, 32, 5919. (b) W. H. Pearson, R. Walavalkar, Tetrahedron Lett., 1994, 50, 12293. (c) M. A. Ciufolini, F. Roschangar, J. Am. Chem. Soc., 1996, 118, 12082. (d) D. L. Comins, X. Chen, L. A. Morgan, J. Org. Chem., 1997, 62, 7435.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 5919
    • Comins, D.L.1    Morgan, L.A.2
  • 4
    • 0027974072 scopus 로고
    • For recent reviews, see: Z. Li, Z. Jin, R. Huang, Synthesis, 2001, 2365. For recent synthesis of tylophorine also see: (a) D. L. Comins, L. A. Morgan, Tetrahedron Lett., 1991, 32, 5919. (b) W. H. Pearson, R. Walavalkar, Tetrahedron Lett., 1994, 50, 12293. (c) M. A. Ciufolini, F. Roschangar, J. Am. Chem. Soc., 1996, 118, 12082. (d) D. L. Comins, X. Chen, L. A. Morgan, J. Org. Chem., 1997, 62, 7435.
    • (1994) Tetrahedron Lett. , vol.50 , pp. 12293
    • Pearson, W.H.1    Walavalkar, R.2
  • 5
    • 0030474491 scopus 로고    scopus 로고
    • For recent reviews, see: Z. Li, Z. Jin, R. Huang, Synthesis, 2001, 2365. For recent synthesis of tylophorine also see: (a) D. L. Comins, L. A. Morgan, Tetrahedron Lett., 1991, 32, 5919. (b) W. H. Pearson, R. Walavalkar, Tetrahedron Lett., 1994, 50, 12293. (c) M. A. Ciufolini, F. Roschangar, J. Am. Chem. Soc., 1996, 118, 12082. (d) D. L. Comins, X. Chen, L. A. Morgan, J. Org. Chem., 1997, 62, 7435.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 12082
    • Ciufolini, M.A.1    Roschangar, F.2
  • 6
    • 1542396379 scopus 로고    scopus 로고
    • For recent reviews, see: Z. Li, Z. Jin, R. Huang, Synthesis, 2001, 2365. For recent synthesis of tylophorine also see: (a) D. L. Comins, L. A. Morgan, Tetrahedron Lett., 1991, 32, 5919. (b) W. H. Pearson, R. Walavalkar, Tetrahedron Lett., 1994, 50, 12293. (c) M. A. Ciufolini, F. Roschangar, J. Am. Chem. Soc., 1996, 118, 12082. (d) D. L. Comins, X. Chen, L. A. Morgan, J. Org. Chem., 1997, 62, 7435.
    • (1997) J. Org. Chem. , vol.62 , pp. 7435
    • Comins, D.L.1    Chen, X.2    Morgan, L.A.3
  • 8
    • 7244235198 scopus 로고    scopus 로고
    • note
    • Amino alcohol 12 is extremely sensitive to light. All operations should carry out rapidly and avoid exposing to light.
  • 9
    • 7244253884 scopus 로고    scopus 로고
    • note
    • 4 C, 73.26; H, 6.92; N 3.56; Found. C, 73.38; H, 6.60; N, 3.55.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.