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Volumn 131, Issue 47, 2009, Pages 17074-17075

Palladium-catalyzed enantioselective addition of two distinct nucleophiles across alkenes capable of quinone methide formation

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; CHIRAL CENTERS; DIASTEREOMERIC RATIOS; DIFUNCTIONALIZATION; ENANTIOMERIC RATIO; ENANTIOSELECTIVE; ENANTIOSELECTIVE ADDITION; HETEROCYCLIC COMPOUND; QUINONE METHIDE;

EID: 72249086147     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja909030c     Document Type: Article
Times cited : (143)

References (35)
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    • For a review of pioneering work in this area, see: (a) 2nd ed.; Wiley-VCH: Weinheim
    • For a review of pioneering work in this area, see: (a) Bäckvall, J.-E. Metal-Catalyzed Cross-Coupling Reactions, 2nd ed.; Wiley-VCH: Weinheim, 2004; Vol.2, p 479.
    • (2004) Metal-Catalyzed Cross-Coupling Reactions , vol.2 , pp. 479
    • Bäckvall, J.-E.1
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    • For a leading reference on alkoxycarbonylation, see: (c)
    • For a leading reference on alkoxycarbonylation, see: (c) Semmelhack, M. F.; Bodurow, C. J. Am. Chem. Soc. 1984, 106, 1496.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 1496
    • Semmelhack, M.F.1    Bodurow, C.2
  • 15
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    • For a review of advances in Pd-catalyzed alkene difunctionalization, see: (d)
    • For a review of advances in Pd-catalyzed alkene difunctionalization, see: (d) Jensen, K. H.; Sigman, M. S. Org. Biomol. Chem. 2008, 6, 4083.
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 4083
    • Jensen, K.H.1    Sigman, M.S.2
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    • For other examples of Pd-catalyzed dioxygenation of o-vinyl phenols, see: (c)
    • For other examples of Pd-catalyzed dioxygenation of o-vinyl phenols, see: (c) Chevrin, C.; Le Bras, J.; Henin, F.; Muzart, J. Synthesis 2005, 2615.
    • (2005) Synthesis , pp. 2615
    • Chevrin, C.1    Le Bras, J.2    Henin, F.3    Muzart, J.4
  • 27
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    • note
    • E- and Z-alkene isomers are observed to isomerize rapidly under the reaction conditions, and thus a mixture of isomers is allowed.
  • 28
    • 72249113602 scopus 로고    scopus 로고
    • note
    • This experiment results in a complex mixture of uncharacterized byproducts believed to be a result of oligomerization.
  • 31
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    • note
    • See Supporting Information for details.
  • 32
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    • note
    • 9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.