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Volumn 1, Issue 6, 2006, Pages 894-904

Synthesis of murisolin, (15R, 16R, 19R, 20S)-murisolin A, and (15R, 16R, 19S, 20S)-16,19-cis-murisolin and their inhibitory action with bovine heart mitochondrial complex I

Author keywords

Annonaceous acetogenins; Antitumor agents; Mitochondrial complex I; Natural products; Total synthesis

Indexed keywords

ENZYME INHIBITOR; FURAN DERIVATIVE; LACTONE; MURISOLIN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); UNCLASSIFIED DRUG;

EID: 33845922401     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.200600261     Document Type: Article
Times cited : (25)

References (35)
  • 4
    • 33747291925 scopus 로고    scopus 로고
    • For recent total syntheses of mono-THF acetogenins, see: a
    • For recent total syntheses of mono-THF acetogenins, see: a) H. Göksel, C. B. W. Stark, Org. Lett. 2006, 8, 3433-3436;
    • (2006) Org. Lett , vol.8 , pp. 3433-3436
    • Göksel, H.1    Stark, C.B.W.2
  • 16
    • 27544434009 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 6938-6940.
    • (2005) Chem. Int. Ed , vol.44 , pp. 6938-6940
    • Angew1
  • 30
    • 0027985492 scopus 로고    scopus 로고
    • The absolute configurations at C4 and C34 were well-known and determined to be R and S, respectively; see: T. R. Hoye, P. R. Hanson, L. E. Hasenwinkel, E. A. Ramirez, Z. P. Zhuang, Tetrahedron Lett. 1994, 35, 8529-8532.
    • The absolute configurations at C4 and C34 were well-known and determined to be R and S, respectively; see: T. R. Hoye, P. R. Hanson, L. E. Hasenwinkel, E. A. Ramirez, Z. P. Zhuang, Tetrahedron Lett. 1994, 35, 8529-8532.
  • 31
    • 33845941999 scopus 로고    scopus 로고
    • Tanaka and co-workers also prepared 3b. Its melting point was reported to be 65-66 °C.[5b]
    • Tanaka and co-workers also prepared 3b. Its melting point was reported to be 65-66 °C.[5b]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.