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Volumn 105, Issue 12, 2005, Pages 4661-4670

Total synthesis of ingenol

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; ESTERS; HYDROXYLATION; ISOMERS; MOLECULAR STRUCTURE; OXYGEN; PROTEINS; STEREOCHEMISTRY;

EID: 30744431862     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr040636z     Document Type: Review
Times cited : (66)

References (58)
  • 12
    • 0000560130 scopus 로고    scopus 로고
    • For a review on inside-outside chemistry, see
    • For a review on inside-outside chemistry, see: Alder, R. W.; East, S. P. Chem. Rev. 1996, 96, 2097.
    • (1996) Chem. Rev. , vol.96 , pp. 2097
    • Alder, R.W.1    East, S.P.2
  • 13
    • 30744441230 scopus 로고    scopus 로고
    • note
    • The ingenane numbering system, as illustrated in Figure 1, is used throughout.
  • 15
    • 0006957213 scopus 로고
    • For reviews on synthetic studies of ingenol and related compounds see
    • For reviews on synthetic studies of ingenol and related compounds, see: (a) Rigby, J. H. Stud. Nat. Prod. Chem. 1993, 12, 233.
    • (1993) Stud. Nat. Prod. Chem. , vol.12 , pp. 233
    • Rigby, J.H.1
  • 32
    • 0001647186 scopus 로고    scopus 로고
    • Application to taxane synthesis, see
    • (b) Tu, Y. Q.; Sun, L. D.; Wang, P. Z. J. Org. Chem. 1999, 64, 629. Application to taxane synthesis, see:
    • (1999) J. Org. Chem. , vol.64 , pp. 629
    • Tu, Y.Q.1    Sun, L.D.2    Wang, P.Z.3
  • 56
    • 30744432184 scopus 로고    scopus 로고
    • note
    • We are indebted to Professor G. Appendino (Dipartimento di Scienze e Tecnologia del Farmaco) for providing natural ingenol.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.