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Volumn 17, Issue 24, 2006, Pages 3341-3350

Reversing Dane's strategy: a new, concise, enantioselective synthesis of the steroid nucleus

Author keywords

[No Author keywords available]

Indexed keywords

STEROID;

EID: 33846581559     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.01.001     Document Type: Article
Times cited : (8)

References (39)
  • 1
    • 84977687749 scopus 로고
    • This work appeared less than a decade after Diels' and Alder's first paper on their reaction. See also:
    • Dane E., Höss O., Bindseil A.W., and Schmitt J. Liebigs Ann. Chem. 532 (1937) 39 This work appeared less than a decade after Diels' and Alder's first paper on their reaction. See also:
    • (1937) Liebigs Ann. Chem. , vol.532 , pp. 39
    • Dane, E.1    Höss, O.2    Bindseil, A.W.3    Schmitt, J.4
  • 2
    • 0011161194 scopus 로고
    • and references cited therein
    • Dane E. Angew. Chem. 52 (1939) 655 and references cited therein
    • (1939) Angew. Chem. , vol.52 , pp. 655
    • Dane, E.1
  • 6
    • 0024500341 scopus 로고
    • For a related approach applied to the synthesis of certain abietanoid pigments, see:
    • For a related approach applied to the synthesis of certain abietanoid pigments, see:. Lee J., and Snyder J.K. J. Am. Chem. Soc. 111 (1989) 1522
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 1522
    • Lee, J.1    Snyder, J.K.2
  • 13
    • 32044461762 scopus 로고    scopus 로고
    • Angew. Chem. 113 (2001) 4198
    • (2001) Angew. Chem. , vol.113 , pp. 4198
  • 16
    • 1842483218 scopus 로고    scopus 로고
    • For recent reviews on enyne metathesis which also include tandem RCEM/Diels-Alder processes, see:
    • For recent reviews on enyne metathesis which also include tandem RCEM/Diels-Alder processes, see:. Diver S.T., and Giessert A.J. Chem. Rev. 104 (2004) 1317
    • (2004) Chem. Rev. , vol.104 , pp. 1317
    • Diver, S.T.1    Giessert, A.J.2
  • 33
    • 33846618754 scopus 로고    scopus 로고
    • note
    • The relative stereochemistry of the major diastereomeric adduct for the cycloadditions of (i) 5a with 6b and (ii) 4b with 11 were each chemically correlated. Thus silylation of 9b gave a compound identical to 10b. Desilylation of 8a gave a compound identical to 7a.
  • 35
    • 33646536570 scopus 로고    scopus 로고
    • Prepared by anti-aldol addition of 1 to 2c followed by RCEM. For our new anti-aldol protocol see:
    • Prepared by anti-aldol addition of 1 to 2c followed by RCEM. For our new anti-aldol protocol see:. Fraser B.H., Gelman D.M., Perlmutter P., and Vounatsos F. Tetrahedron: Asymmetry 17 (2006) 1152
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1152
    • Fraser, B.H.1    Gelman, D.M.2    Perlmutter, P.3    Vounatsos, F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.