메뉴 건너뛰기




Volumn 72, Issue 13, 2007, Pages 4826-4831

Synthesis of chinensines A-E

Author keywords

[No Author keywords available]

Indexed keywords

CHINENSINES D; CORONARIN E; SINGLET OXYGEN;

EID: 34250838591     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo070527v     Document Type: Article
Times cited : (20)

References (35)
  • 5
    • 34250827933 scopus 로고    scopus 로고
    • We have assigned the names chinensine A, B, C, D, and E to compounds 5, 6, 7, 8, and 9, respectively, for ease of discussion. Please note that coronarin E (4) was known and named prior to the isolation of the chinensine family, see refs 1 and 9 and references therein
    • We have assigned the names chinensine A, B, C, D, and E to compounds 5, 6, 7, 8, and 9, respectively, for ease of discussion. Please note that coronarin E (4) was known and named prior to the isolation of the chinensine family, see refs 1 and 9 and references therein.
  • 16
    • 46549101863 scopus 로고
    • For the first isolation of reasonable quantities of highly sensitive furan endoperoxides see: a
    • For the first isolation of reasonable quantities of highly sensitive furan endoperoxides see: (a) Gollnick, K.; Griesbeck, A. Tetrahedron 1985, 41, 2057-2068.
    • (1985) Tetrahedron , vol.41 , pp. 2057-2068
    • Gollnick, K.1    Griesbeck, A.2
  • 22
    • 13444254012 scopus 로고    scopus 로고
    • For reports of similar failures with these methods see
    • For reports of similar failures with these methods see: Kolympadi, M.; Liapis, M.; Ragoussis, V. Tetrahedron 2005, 61, 2003-2010.
    • (2005) Tetrahedron , vol.61 , pp. 2003-2010
    • Kolympadi, M.1    Liapis, M.2    Ragoussis, V.3
  • 25
    • 0008592260 scopus 로고
    • For the silyl stabilization concept, see
    • For the silyl stabilization concept, see: Adam, W.; Rodriguez, A. Tetrahedron Lett. 1981, 22, 3505-3508.
    • (1981) Tetrahedron Lett , vol.22 , pp. 3505-3508
    • Adam, W.1    Rodriguez, A.2
  • 26
    • 0028031384 scopus 로고
    • For direct comparisons between the photoxygenations of silyl-substituted and unsubstituted furans, see: a
    • For direct comparisons between the photoxygenations of silyl-substituted and unsubstituted furans, see: (a) Bury, P.; Hareau, G.; Kocieński, P.; Dhanak, D. Tetrahedron 1994, 50, 8793-8808.
    • (1994) Tetrahedron , vol.50 , pp. 8793-8808
    • Bury, P.1    Hareau, G.2    Kocieński, P.3    Dhanak, D.4
  • 29
    • 0028251491 scopus 로고    scopus 로고
    • Compound 16 is also a natural product: (a) Nakatani, N.; Kikuzaki, H.; Yamaji, H.; Yoshio, K.; Kitora, C.; Okada, K.; Padolina, W. G. Phytochemistry 1994, 37, 1383-1388.
    • Compound 16 is also a natural product: (a) Nakatani, N.; Kikuzaki, H.; Yamaji, H.; Yoshio, K.; Kitora, C.; Okada, K.; Padolina, W. G. Phytochemistry 1994, 37, 1383-1388.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.