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Volumn 76, Issue 7, 2011, Pages 2257-2260

Synthesis of (-)-homogalanthamine from naltrexone

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCHOLINESTERASE; GROB FRAGMENTATION; KEY REACTIONS; NALTREXONE; SYNTHESIS FEATURES; TOTAL YIELD;

EID: 79953227003     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1022487     Document Type: Article
Times cited : (16)

References (49)
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    • (1987) The Alkaloids , vol.30 , pp. 251-376
    • Martin, S.F.1    Brossi, A.2
  • 2
    • 77956708370 scopus 로고    scopus 로고
    • In;, Ed.; Academic Press: New York,; Vol., pp .
    • Hoshino, O. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 1998; Vol. 51, pp 323 - 424.
    • (1998) The Alkaloids , vol.51 , pp. 323-424
    • Hoshino, O.1    Cordell, G.A.2
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    • U.S. Patent 4478840.
    • Smith, D. H., Jr. U.S. Patent 4478840, 1984.
    • (1984)
    • Smith Jr., D.H.1
  • 29
    • 0020673714 scopus 로고
    • Hydroxy-directed reduction of α- or β-hydroxy ketones
    • Hydroxy-directed reduction of α- or β-hydroxy ketones: Saksena, A. K.; Mangiaracina, P. Tetrahedron Lett. 1983, 24, 273
    • (1983) Tetrahedron Lett. , vol.24 , pp. 273
    • Saksena, A.K.1    Mangiaracina, P.2
  • 39
    • 79953191749 scopus 로고    scopus 로고
    • The addition of 15-crown-5 exhibited a crucial effect for the smooth progression of the fragmentation. See the Supporting Information for details.
    • The addition of 15-crown-5 exhibited a crucial effect for the smooth progression of the fragmentation. See the Supporting Information for details.
  • 40
    • 79953232318 scopus 로고    scopus 로고
    • Saegusa oxidation of 4 also provided 17. See the Supporting Information for details.
    • Saegusa oxidation of 4 also provided 17. See the Supporting Information for details.
  • 48
    • 46249124540 scopus 로고    scopus 로고
    • Recently, a demethylation with dodecylthiolate was reported.
    • Recently, a demethylation with dodecylthiolate was reported. Chae, J. Arch. Pharm. Res. 2008, 31, 305
    • (2008) Arch. Pharm. Res. , vol.31 , pp. 305
    • Chae, J.1
  • 49
    • 79953205516 scopus 로고    scopus 로고
    • In general, derivatives with a phenolic OH group show higher affinities for the opioid receptors than the corresponding compounds with a OMe group.
    • In general, derivatives with a phenolic OH group show higher affinities for the opioid receptors than the corresponding compounds with a OMe group.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.