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Volumn 121, Issue 20, 1999, Pages 4900-4901

Synthesis of (-)-histrionicotoxin by a tandem process [5]

Author keywords

[No Author keywords available]

Indexed keywords

HISTRIONICOTOXIN;

EID: 0033606247     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja990138l     Document Type: Letter
Times cited : (99)

References (29)
  • 4
    • 0032474797 scopus 로고    scopus 로고
    • and references therein
    • Tanner, D.; Hagberg, L. Tetrahedron 1998, 54, 7907 and references therein.
    • (1998) Tetrahedron , vol.54 , pp. 7907
    • Tanner, D.1    Hagberg, L.2
  • 22
    • 0344311826 scopus 로고    scopus 로고
    • 23 was low-yielding in the presence of the acyl camphor sultam
    • 23 was low-yielding in the presence of the acyl camphor sultam.
  • 24
    • 0037988256 scopus 로고    scopus 로고
    • The cycloreversion of phenyl-substituted isoxazolidines to release cyclic nitrones in situ appears to be novel, although it has recently been used to regenerate a nitrone by flash pyrolysis. See Coskun, N.; Ay, M. Heterocycles 1998, 48, 537.
    • (1998) Heterocycles , vol.48 , pp. 537
    • Coskun, N.1    Ay, M.2
  • 25
    • 0001647908 scopus 로고
    • 2 was used to generate the ylid at -30 °C, and the precipitated potassium salts were then removed to give a salt-free, yellow solution of the ylid which was added via cannula to a solution of the aldehyde in THF at -78 °C
    • 2 was used to generate the ylid at -30 °C, and the precipitated potassium salts were then removed to give a salt-free, yellow solution of the ylid which was added via cannula to a solution of the aldehyde in THF at -78 °C.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2173
    • Stork, G.1    Zhao, K.2
  • 28
    • 0345174276 scopus 로고    scopus 로고
    • Cleavage of the N-O bond in the presence of the desilylated enynes was accompanied by reduction of the acetylenic groups to give a mixture of HTX, dihydro-HTX, neodihydro-HTX, and tetrahydro-HTX
    • Cleavage of the N-O bond in the presence of the desilylated enynes was accompanied by reduction of the acetylenic groups to give a mixture of HTX, dihydro-HTX, neodihydro-HTX, and tetrahydro-HTX.
  • 29
    • 0344744165 scopus 로고    scopus 로고
    • note
    • 2 = 0.837.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.