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Volumn 12, Issue 21, 2010, Pages 5064-5067

Catalytic enantioselective Friedländer condensations: Facile access to quinolines with remote stereogenic centers

Author keywords

[No Author keywords available]

Indexed keywords

QUINOLINE DERIVATIVE;

EID: 78049497552     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1023932     Document Type: Article
Times cited : (50)

References (111)
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    • For selected reviews on aldol reactions, see
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    • For selected reviews on Mannich reactions, see
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    • For selected examples of other reactions, see
  • 64
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    • For enamine-catalyzed desymmetrizations, see
    • For enamine-catalyzed desymmetrizations, see
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    • For examples, see
    • For examples, see
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    • references cited therein
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    • For a review of primary amino acid catalysis, see
    • For a review of primary amino acid catalysis, see
  • 82
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    • Other catalysts such as diarylprolinol, diarylprolinol silyl ether, and proline amide gave inferior results
    • Xu, L.-W.; Lu, Y. Org. Biomol. Chem. 2008, 6, 2047 Other catalysts such as diarylprolinol, diarylprolinol silyl ether, and proline amide gave inferior results
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    • For selected previous uses of these catalysts, see
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    • For instance, the reaction in dichloromethane (dielectric constant = 9.1) took substantially longer to go to completion as compared to the corresponding reaction in dioxane (dielectric constant = 2.2), while giving rise to a similar level of enantioselectivity
    • For instance, the reaction in dichloromethane (dielectric constant = 9.1) took substantially longer to go to completion as compared to the corresponding reaction in dioxane (dielectric constant = 2.2), while giving rise to a similar level of enantioselectivity.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.