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Volumn 12, Issue 7, 2010, Pages 1600-1603

Synthesis of the spiroiminal moiety of marineosins A and B

Author keywords

[No Author keywords available]

Indexed keywords

MARINEOSIN A; MARINEOSIN B; PYRROLE DERIVATIVE; SPIRO COMPOUND;

EID: 77950195860     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol100333d     Document Type: Article
Times cited : (26)

References (14)
  • 8
    • 0041366893 scopus 로고
    • Hydrogenolysis of a keto isoxaoline afforded a compound whose spectral data are in agreement with those of a hemi-iminal. See compound 12 in: Andersen, S. H.; Sharma, K. K.; Torssell, K. B. G. Tetrahedron 1983, 39, 2241-2245.
    • (1983) Tetrahedron , vol.39 , pp. 2241-2245
    • Andersen, S.H.1    Sharma, K.K.2    Torssell, K.B.G.3
  • 10
    • 0004419437 scopus 로고
    • Cycloadditions with the nitrile N-oxide derived from benzaldehyde oxime can be carried out at room temperature, whereas diose with the nitrile N-oxide derived from the oxime of pyrrole-2-carboxaldehyde must be carried out at -70 °C See: Ghabrial, S. S.; Thomsen, I.; Torssell, K. B. G. Acta chem. Scand. B 1987, B41, 426-434.
    • (1987) Acta Chem. Scand. B , vol.B41 , pp. 426-434
    • Ghabrial, S.S.1    Thomsen, I.2    Torssell, K.B.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.