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Volumn 12, Issue 13, 2006, Pages 3647-3654

Diastereoselective synthesis of highly functionalized tetrahydroxanthenols - Unprecedented access to privileged structural motifs

Author keywords

Domino reactions; Oxidation; Polyols; Tetrahydroxanthenones

Indexed keywords

CONDENSATION REACTIONS; CRYSTAL STRUCTURE; OXIDATION; STEREOCHEMISTRY;

EID: 33646172408     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200501485     Document Type: Article
Times cited : (35)

References (48)
  • 14
    • 0003709372 scopus 로고    scopus 로고
    • (Eds.: M. Nelson, W. Hillen, R. A. Greenwald), Birkhauser, Boston
    • a) Tetracyclines in Biology, Chemistry and Medicine (Eds.: M. Nelson, W. Hillen, R. A. Greenwald), Birkhauser, Boston, 2001;
    • (2001) Tetracyclines in Biology, Chemistry and Medicine
  • 21
    • 7044235263 scopus 로고    scopus 로고
    • For a review on domino reactions see : L. F. Tietze, Chem. Rev. 1996, 96, 115-136.
    • (1996) Chem. Rev. , vol.96 , pp. 115-136
    • Tietze, L.F.1
  • 43
    • 0025788674 scopus 로고
    • For the discussion of hydrogen bonding during epoxidations of cycloalkenols see: a) C. M. Marson, D. W. M. Benzies, A. D. Hobson, Tetrahedron 1991, 47, 5491-5506;
    • (1991) Tetrahedron , vol.47 , pp. 5491-5506
    • Marson, C.M.1    Benzies, D.W.M.2    Hobson, A.D.3
  • 45
    • 33646183526 scopus 로고    scopus 로고
    • note
    • c) a simple control experiment with mCPBA in ethanol only led to partial decomposition of the starting material.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.