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Volumn 71, Issue 19, 2006, Pages 7354-7363

Total synthesis of the 7,3′-linked naphthylisoquinoline alkaloid ancistrocladidine

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; LEAD; MIXTURES; NITROGEN COMPOUNDS; RECRYSTALLIZATION (METALLURGY); SYNTHESIS (CHEMICAL);

EID: 33749031542     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0611364     Document Type: Article
Times cited : (17)

References (88)
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    • The groups of Pinhey and Barton have shown that this is an efficient method for the generation of extremely hindered biaryl linkages: (a) Bell, H. C.; Pinhey, J. T.; Sternhell, S. Aust. J. Chem. 1979, 32, 1551-1560.
    • (1979) Aust. J. Chem. , vol.32 , pp. 1551-1560
    • Bell, H.C.1    Pinhey, J.T.2    Sternhell, S.3
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    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford
    • (e) Pinhey, J. T. In Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, 1995; Vol. 11, p 461.
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    • Pinhey, J.T.1
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    • A preliminary communication of this work has been published: Bungard, C. J.; Morris, J. C. Org. Lett. 2002, 4, 631-633.
    • (2002) Org. Lett. , vol.4 , pp. 631-633
    • Bungard, C.J.1    Morris, J.C.2
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    • (c) Kozyrod, R. P.; Morgan, J.; Pinhey, J. 1985, 38, 1147.
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    • The aldehyde 8 is readily available from 3,5-dihydroxybenzoic acid as described in (a) Gray, J. S.; Martin, G. C. J.; Rigby, W. J. Chem. Soc. C 1967, 2580-2587.
    • (1967) J. Chem. Soc. C , pp. 2580-2587
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    • workbench ed. E21: Georg Thieme Verlag: Stuttgart
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    • The diasteromeric excess of this reaction was determined by the method described in Dale, J. A.; Dull, D. L.; Mosher, H. S. J. Org. Chem. 1969, 34, 2543-2549. Details are provided in Supporting Information.
    • (1969) J. Org. Chem. , vol.34 , pp. 2543-2549
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    • note
    • General procedures are detailed in Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.