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Volumn , Issue 3, 2000, Pages 439-448

Studies towards the synthesis of aplykurodins - Synthesis of 17,18- dihydro-3,9-di-epi-aplykurodinone B

Author keywords

Aplykurodins; Cyclic peroxides; Lactonization; Marine steroids; Stille reaction

Indexed keywords

ALLYL ALCOHOL; COLECALCIFEROL; KETONE; LACTONE DERIVATIVE;

EID: 0033952072     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(200002)2000:3<439::aid-ejoc439>3.0.co;2-f     Document Type: Article
Times cited : (5)

References (29)
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    • note
    • It is known that anaspidean mollusks of the family Aplysiidae are known to have few predators. Moreover, biological testing on other members of this class of compounds [(17R)-17-methyl-incisterol and derivatives] shows interesting in vitro activities: I. Izzo, PhD thesis, University of Salerno.
  • 8
    • 0000994355 scopus 로고
    • synthesis of Grundmann ketone
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  • 9
    • 0001282465 scopus 로고
    • C. A. Hoeger, W. H. Okamura, J. Am. Chem. Soc. 1985, 107, 268; B. Fernàndez, J. A. Martìnez Perez, J. R. Granja, L. Castedo, A. Mouriño, J. Org. Chem. 1992, 57, 3173; synthesis of 13.
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    • Hoeger, C.A.1    Okamura, W.H.2
  • 18
    • 85086352388 scopus 로고    scopus 로고
    • note
    • 2 and LDA, gave extensive decomposition of the starting material and/or elimination of the MEM-oxy group to yield the α,β-unsaturated ketone 12.
  • 20
    • 33845557937 scopus 로고
    • M. Balci, Chem. Rev. 1981, 81, 91; E. Demole, C. Demole, D. Berthet, Helv. Chim. Acta 1973, 56, 275; N. W. Danny, A. Nickon, Org. React. 1973, 20, 133.
    • (1981) Chem. Rev. , vol.81 , pp. 91
    • Balci, M.1
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  • 22
    • 0001347157 scopus 로고
    • M. Balci, Chem. Rev. 1981, 81, 91; E. Demole, C. Demole, D. Berthet, Helv. Chim. Acta 1973, 56, 275; N. W. Danny, A. Nickon, Org. React. 1973, 20, 133.
    • (1973) Org. React. , vol.20 , pp. 133
    • Danny, N.W.1    Nickon, A.2
  • 26
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    • and references cited therein
    • It is generally believed that in the hydrindanone systems, the cis isomers are more stable than the trans isomers. However, there are many cases where the more stable isomer is the trans one. See: M. Tori, M. Ikawa, T. Sagawa, H. Furuta, M. Sono, Y. Asakawa, Tetrahedron 1996, 50, 9999 and references cited therein.
    • (1996) Tetrahedron , vol.50 , pp. 9999
    • Tori, M.1    Ikawa, M.2    Sagawa, T.3    Furuta, H.4    Sono, M.5    Asakawa, Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.