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Volumn 137, Issue 22, 2015, Pages 7128-7134

Iron-Catalyzed Enantioselective Cross-Coupling Reactions of α-Chloroesters with Aryl Grignard Reagents

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CHEMICAL BONDS; CHEMICAL REACTIONS; IRON; IRON COMPOUNDS; ORGANOMETALLICS; STEREOCHEMISTRY;

EID: 84935855432     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.5b02277     Document Type: Article
Times cited : (182)

References (80)
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    • (2012) Comprehensive Chirality , vol.4 , pp. 18
    • Uozumi, Y.1
  • 2
    • 84919690663 scopus 로고    scopus 로고
    • Andrushko, V., Andrushko, N., Eds.; John Wiley and Sons, Inc.: Hoboken, NJ
    • Sarli, V. In Stereoselective Synthesis of Drug and Natural Products; Andrushko, V., Andrushko, N., Eds.; John Wiley and Sons, Inc.: Hoboken, NJ, 2013; Vol. 1, p 369.
    • (2013) Stereoselective Synthesis of Drug and Natural Products , vol.1 , pp. 369
    • Sarli, V.1
  • 62
    • 84935859402 scopus 로고    scopus 로고
    • note
    • Dexibuprofen and naproxen are optically active nonsteroidal anti-inflammatory drugs and are commonly used for clinical purposes.
  • 63
    • 84935869907 scopus 로고    scopus 로고
    • note
    • 3 was reduced to an Fe(II) species.
  • 80
    • 84935890824 scopus 로고    scopus 로고
    • note
    • A similar radical probe containing a geometrically defined terminal (Z)-alkene moiety also provided a mixture of the corresponding uncyclized and cyclized products. The (Z) stereochemistry of the uncyclized product and the recovered halide substrate did not isomerize to the (E)-alkene during the reaction, indicating the radical cyclization of 7 to 7′ was irreversible. See the Supporting Information for details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.