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Volumn 14, Issue 11, 2012, Pages 2714-2717

Total synthesis of (-)-galanthamine and (-)-lycoramine via catalytic asymmetric hydrogenation and intramolecular reductive Heck cyclization

Author keywords

[No Author keywords available]

Indexed keywords

AMARYLLIDACEAE ALKALOID; GALANTAMINE; LYCORAMINE; PALLADIUM; RUTHENIUM;

EID: 84861838551     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol300913g     Document Type: Article
Times cited : (106)

References (36)
  • 16
    • 27144524460 scopus 로고    scopus 로고
    • Catalytic asymmetric synthesis of (-)-galanthamine (10 steps, 8% overall yield)
    • Trost, B. M.; Tang, W.; Toste, F. D. J. Am. Chem. Soc. 2005, 127, 14785 Catalytic asymmetric synthesis of (-)-galanthamine (10 steps, 8% overall yield).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 14785
    • Trost, B.M.1    Tang, W.2    Toste, F.D.3
  • 21
    • 84861822681 scopus 로고    scopus 로고
    • Catalytic asymmetric synthesis of (-)-galanthamine (16 steps, 2.8% overall yield) and (-)-lycoramine (14 steps, 8.1% overall yield)
    • Chen, P.; Bao, X.; Zhang, L.-F.; Ding, M.; Han, X.-J.; Li, J.; Zhang, G.-B.; Tu, Y.-Q.; Fan, C.-A. Angew. Chem., Int. Ed. 2011, 50, 8186 Catalytic asymmetric synthesis of (-)-galanthamine (16 steps, 2.8% overall yield) and (-)-lycoramine (14 steps, 8.1% overall yield).
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 8186
    • Chen, P.1    Bao, X.2    Zhang, L.-F.3    Ding, M.4    Han, X.-J.5    Li, J.6    Zhang, G.-B.7    Tu, Y.-Q.8    Fan, C.-A.9
  • 24
    • 0003441482 scopus 로고
    • John Wiley: New York, Selected papers for intramolecular reductive Heck reaction for the construction of dihydrobenzofuran ring
    • Tsuji, J. Palladium Reagent and Catalysts. Innovation in Organic Synthesis; John Wiley: New York, 1995. Selected papers for intramolecular reductive Heck reaction for the construction of dihydrobenzofuran ring
    • (1995) Palladium Reagent and Catalysts. Innovation in Organic Synthesis
    • Tsuji, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.