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Volumn 70, Issue 23, 2005, Pages 9486-9494

Asymmetric synthesis of tetrahydropalmatine via tandem 1,2-addition/ cyclization

Author keywords

[No Author keywords available]

Indexed keywords

FRIEDEL-CRAFTS REACTION; PURIFICATION; STEREOCHEMISTRY; SUBSTRATES; SYNTHESIS (CHEMICAL);

EID: 27744533660     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo051554t     Document Type: Article
Times cited : (54)

References (55)
  • 2
    • 0010961967 scopus 로고
    • Manske, R. H. F., Rodrigo, R. G. A., Eds.; Academic Press: New York
    • (b) Santavy, F. In The Alkaloids: Chemistry and Physiology; Manske, R. H. F., Rodrigo, R. G. A., Eds.; Academic Press: New York, 1979; Vol. 17, 385.
    • (1979) The Alkaloids: Chemistry and Physiology , vol.17 , pp. 385
    • Santavy, F.1
  • 3
    • 77957049399 scopus 로고
    • Manske, R. H. F., Ed.; Academic Press: New York
    • (c) Šantavý, F. In The Alkaloids: Chemistry and Physiology; Manske, R. H. F., Ed.; Academic Press: New York, 1970; Vol. 12, p 333.
    • (1970) The Alkaloids: Chemistry and Physiology , vol.12 , pp. 333
    • Šantavý, F.1
  • 4
    • 0008516907 scopus 로고
    • Manske, R. H. F., Ed.; Academic Press: New York
    • (d) Jeffs, P. W. In The Alkaloids: Chemistry and Physiology; Manske, R. H. F., Ed.; Academic Press: New York, 1967; Vol. 9, p 41.
    • (1967) The Alkaloids: Chemistry and Physiology , vol.9 , pp. 41
    • Jeffs, P.W.1
  • 7
    • 0002269682 scopus 로고
    • Brossi, A., Ed.; Academic Press: Orlando, FL
    • (b) Suffnees, M.; Cordeil, A. C. In The Alkaloids; Brossi, A., Ed.; Academic Press: Orlando, FL, 1985; Vol. 25, p 3.
    • (1985) The Alkaloids , vol.25 , pp. 3
    • Suffnees, M.1    Cordeil, A.C.2
  • 12
    • 4243241249 scopus 로고
    • For a review on Pictet-Spengler cyclization, see: Cox, E. D.; Cook, J. M. Chem. Rev. 1995, 95, 1797.
    • (1995) Chem. Rev. , vol.95 , pp. 1797
    • Cox, E.D.1    Cook, J.M.2
  • 37
    • 17244378815 scopus 로고    scopus 로고
    • For recent reviews on the SAMP/RAMP-hydrazone method, see: (a) Enders, D.; Voith, M.; Lenzen, A. Angew. Chem. 2005, 117, 1330;
    • (2005) Angew. Chem. , vol.117 , pp. 1330
    • Enders, D.1    Voith, M.2    Lenzen, A.3
  • 45
    • 27744562529 scopus 로고    scopus 로고
    • note
    • 2O. This resulted in an increase of the yield from 70 to 80%.
  • 47
    • 27744556561 scopus 로고    scopus 로고
    • note
    • 3N and 1.1 equiv of MsCl to a solution of 2-((S)-3-phenyl-3,4- dihydro-1H-isoquinolin-2-yl)-ethanol in absence of LiCl.
  • 48


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.