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Volumn 58, Issue 25, 1993, Pages 7195-7203

Total Synthesis and Structure Assignment of the Antitumor Antibiotic Aranorosin

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC ANTIBIOTIC; ARANOROSIN;

EID: 0027772653     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00077a050     Document Type: Article
Times cited : (103)

References (50)
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    • We have previously applied oxidative cyclizations of tyrosines toward the synthesis of Stemona alkaloids: Wipf, P.; Kim, Y. Tetrahedron Lett. 1992, 33, 5477.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 5477
    • Wipf, P.1    Kim, Y.2
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    • For a preliminary communication on the core structure of aranorosin from this laboratory, see
    • For a preliminary communication on the core structure of aranorosin from this laboratory, see: Wipf, P.; Kim, Y. J. Org. Chem. 1993, 58, 1649.
    • (1993) J. Org. Chem. , vol.58 , pp. 1649
    • Wipf, P.1    Kim, Y.2
  • 7
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    • For other efforts toward the synthesis of aranorosin, see
    • For other efforts toward the synthesis of aranorosin, see: Rama Rao, A. V.; Gurjar, M. K.; Sharma, P. A. Tetrahedron Lett. 1991, 32, 6613.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 6613
    • Rama Rao, A.V.1    Gurjar, M.K.2    Sharma, P.A.3
  • 32
    • 85022567739 scopus 로고
    • Several structurally related dienones show complete planarity in the solid state
    • Several structurally related dienones show complete planarity in the solid state: Pilotti, A.-M. Acta Crystallogr. 1972. B28, 2123.
    • (1972) Acta Crystallogr. , vol.B28 , pp. 2123
    • Pilotti, A.-M.1
  • 34
    • 0000110756 scopus 로고
    • For a recent scholarly analysis of steric effects in the diastereo-selective addition to chiral aldehydes, see
    • For a recent scholarly analysis of steric effects in the diastereo-selective addition to chiral aldehydes, see; Lodge, E. P.; Heathcock, C. H. J. Am. Chem. Soc. 1987, 109, 3353.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 3353
    • Lodge, E.P.1    Heathcock, C.H.2
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    • For a discussion of the torsional strain model in the nucleophilic 1,2-addition to cyclohexenones, see
    • For a discussion of the torsional strain model in the nucleophilic 1,2-addition to cyclohexenones, see: Wu, Y.-D.; Houk, K. N.; Florez, J.; Trost, B. M. J. Org. Chem. 1991, 56, 3656.
    • (1991) J. Org. Chem. , vol.56 , pp. 3656
    • Wu, Y.-D.1    Houk, K.N.2    Florez, J.3    Trost, B.M.4
  • 36
    • 0001213797 scopus 로고
    • For the use of alkoxide groups for controlling regio- and stereoselectivity in additions to γ-hydroxy enones, see
    • For the use of alkoxide groups for controlling regio- and stereoselectivity in additions to γ-hydroxy enones, see: Fischer, A.; Henderson, G. N. Tetrahedron Lett. 1980, 21, 701.
    • (1980) Tetrahedron Lett. , vol.21 , pp. 701
    • Fischer, A.1    Henderson, G.N.2
  • 46
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    • manuscript in preparation
    • Wipf, P.; Kim, Y., manuscript in preparation.
    • Wipf, P.1    Kim, Y.2
  • 47
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    • For a theoretical analysis of the influence of electrostatic effects in π-facial stereoselection, see
    • For a theoretical analysis of the influence of electrostatic effects in π-facial stereoselection, see: Wong, S. S.; Paddon-Row, M. N. Aust. J. Chem. 1991, 44, 765.
    • (1991) Aust. J. Chem. , vol.44 , pp. 765
    • Wong, S.S.1    Paddon-Row, M.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.