메뉴 건너뛰기




Volumn 6, Issue 3, 2011, Pages 786-790

A practical synthesis of cephalostatin 1

Author keywords

cephalostatin 1; natural products; spiroketal; steroids; synthesis design

Indexed keywords

CEPHALOSTATIN 1; NATURAL PRODUCTS; SPIROKETAL; STEROIDS; SYNTHESIS DESIGN;

EID: 79951966663     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201000882     Document Type: Article
Times cited : (37)

References (38)
  • 4
    • 79951989613 scopus 로고    scopus 로고
    • For more synthetic studies from the groups of Fuchs, Heathcock, Winterfeldt, Taber and Shair see ther following and references cited therein
    • For more synthetic studies from the groups of Fuchs, Heathcock, Winterfeldt, Taber and Shair see ther following and references cited therein
  • 11
    • 4243308127 scopus 로고    scopus 로고
    • Chem. Abstr. 1998, 128, 167599 ]
    • (1998) Chem. Abstr. , vol.128 , pp. 167599
  • 13
    • 84899019680 scopus 로고    scopus 로고
    • Chem. Abstr. 2003, 136, 340870 ].
    • (2003) Chem. Abstr. , vol.136 , pp. 340870
  • 15
    • 0035372638 scopus 로고    scopus 로고
    • P. B. Reese, Steroids 2001, 66, 481-497
    • (2001) Steroids , vol.66 , pp. 481-497
    • Reese, P.B.1
  • 19
    • 79951962098 scopus 로고    scopus 로고
    • CCDC 791575 contains the supplementary crystallographic data for 16.These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 791575 contains the supplementary crystallographic data for 16.These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
  • 21
    • 79952000658 scopus 로고    scopus 로고
    • The 23(R) stereochemistry of the major adduct 4 was confirmed by X-ray crystallography of its 3-hydroxyl derivative (CCDC 791577, see Supporting Information)
    • The 23(R) stereochemistry of the major adduct 4 was confirmed by X-ray crystallography of its 3-hydroxyl derivative (CCDC 791577, see Supporting Information).
  • 23
    • 79951975137 scopus 로고    scopus 로고
    • The structure of 22 was confirmed by X-ray crystallography of its 3-silyl ether derivative (CCDC 791576, see Supporting Information)
    • The structure of 22 was confirmed by X-ray crystallography of its 3-silyl ether derivative (CCDC 791576, see Supporting Information).
  • 27
    • 79951999722 scopus 로고    scopus 로고
    • See Supporting Information for the synthesis of chiral aldehyde 27
    • See Supporting Information for the synthesis of chiral aldehyde 27.
  • 32
    • 79951984977 scopus 로고    scopus 로고
    • Thioketal could be unmasked under cycloaddtion conditions, while removal of acid-sensitive protecting groups and E/F-ring ketalization could take place simultaneously during reductive cleavage of the O-O bond (Zn powder in HOAc)
    • Thioketal could be unmasked under cycloaddtion conditions, while removal of acid-sensitive protecting groups and E/F-ring ketalization could take place simultaneously during reductive cleavage of the O-O bond (Zn powder in HOAc).
  • 34
    • 25444498936 scopus 로고    scopus 로고
    • N2' reaction to complete the functionalization of the D ring as the key transformation in their synthesis of south 7 hemisphere
    • N2' reaction to complete the functionalization of the D ring as the key transformation in their synthesis of south 7 hemisphere:, J. S. Lee, P. L. Fuchs, J. Am. Chem. Soc. 2005, 127, 13122-13123.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 13122-13123
    • Lee, J.S.1    Fuchs, P.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.