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Volumn 73, Issue 8, 2010, Pages 1427-1430

Enantioselective total synthesis and X-ray structures of the tetrahydroprotoberberine alkaloids (-)-(S)-tetrahydropalmatrubine and (-)-(S)-corytenchine

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID DERIVATIVE; BENZYLTETRAHYDROISOQUINOLINE; BERBINE DERIVATIVE; CORYTENCHINE; INDANIDINE; N NORLAUDANIDINE; QUINOLINE; TETRAHYDROPALMATRUBINE; UNCLASSIFIED DRUG; (S)-TETRAHYDROPALMATRUBINE; BERBERINE DERIVATIVE;

EID: 77956205001     PISSN: 01633864     EISSN: 15206025     Source Type: Journal    
DOI: 10.1021/np1001169     Document Type: Article
Times cited : (19)

References (59)
  • 15
    • 84925570386 scopus 로고    scopus 로고
    • For a review on Pictet-Spengler cyclization, see
    • For a review on Pictet-Spengler cyclization, see
  • 16
    • 4243241249 scopus 로고
    • For examples, see: J. Org. Chem. 1996, 61, 4607-4610
    • Cox, E. D. and Cook, J. M. Chem. Rev. 1995, 95, 1797-1842 For examples, see: Munchoff, M. J. and Meyers, A. I. J. Org. Chem. 1996, 61, 4607-4610
    • (1995) Chem. Rev. , vol.95 , pp. 1797-1842
    • Cox, E.D.1    Cook, J.M.2    Munchoff, M.J.3    Meyers, A.I.4
  • 22
    • 84925567207 scopus 로고    scopus 로고
    • See, for example
    • See, for example
  • 39
    • 84925567206 scopus 로고    scopus 로고
    • For a recent enantioselective synthesis of some benzyltetrahydroisoquinolines via a Bischler-Napieralski approach, see
    • For a recent enantioselective synthesis of some benzyltetrahydroisoquinolines via a Bischler-Napieralski approach, see
  • 42
    • 84925560750 scopus 로고    scopus 로고
    • For earlier applications of (S)- and (R)-α-methylbenzylamine in a Bischler-Napieralski cyclization see e.g.
    • For earlier applications of (S)- and (R)-α-methylbenzylamine in a Bischler-Napieralski cyclization see e.g.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.