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Volumn 45, Issue 21, 2004, Pages 4181-4183

A stannous chloride-induced deacetalisation-cyclisation process to prepare the ABC ring system of 'upenamide

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; CARBON; LACTONE DERIVATIVE; MACROCYCLIC COMPOUND; STANNOUS CHLORIDE; UNCLASSIFIED DRUG; UPENAMIDE;

EID: 2342596531     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.03.119     Document Type: Article
Times cited : (21)

References (16)
  • 2
    • 0001729486 scopus 로고
    • The xestospongins A-D and araguspongines A-J, are distantly related 20-membered acrocycles, although lacking the spiro-cyclic system and the dense functionality:
    • The xestospongins A-D and araguspongines A-J, are distantly related 20-membered acrocycles, although lacking the spiro-cyclic system and the dense functionality: Nakagawa M., Endo M., Tanaka N., Gen-Pei L. Tetrahedron Lett. 25:1984;3227-3230
    • (1984) Tetrahedron Lett. , vol.25 , pp. 3227-3230
    • Nakagawa, M.1    Endo, M.2    Tanaka, N.3    Gen-Pei, L.4
  • 12
    • 2342610827 scopus 로고    scopus 로고
    • note
    • All novel compounds were characterised by high resolution mass spectrometry and IR and NMR spectroscopy (COSY and HMQC experiments were used to assign any ambiguous peaks)
  • 15
    • 2342555866 scopus 로고    scopus 로고
    • note
    • +, 344.2228 (0.6 ppm error)]
  • 16
    • 2342556804 scopus 로고    scopus 로고
    • note
    • Cambridge Crystallographic Data Centre reference no 2341139


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.