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Volumn 52, Issue 31, 2013, Pages 8156-8159

Enantioselective synthesis of quaternary carbon stereogenic centers through copper-catalyzed conjugate additions of aryl- and alkylaluminum reagents to acyclic trisubstituted enones

Author keywords

copper; enantioselective conjugate additions; N heterocyclic carbenes; organoaluminums; quaternary carbons

Indexed keywords

CONJUGATE ADDITION; ENANTIOSELECTIVE CONJUGATE ADDITION; ENANTIOSELECTIVE SYNTHESIS; N-HETEROCYCLIC CARBENES; ORGANOALUMINUM REAGENTS; ORGANOALUMINUMS; QUATERNARY CARBON; STEREOGENIC CENTERS;

EID: 84880792283     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201304035     Document Type: Article
Times cited : (52)

References (51)
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    • For a comprehensive review of enantioselective synthesis of quaternary carbon stereogenic centers within acyclic molecules, see:, J. P. Das, I. Marek, Chem. Commun. 2011, 47, 4593.
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  • 9
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    • A. Wilsily, E. Fillion, J. Org. Chem. 2009, 74, 8583. For related studies involving nitroalkanes as reagents, see
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    • Wilsily, A.1    Fillion, E.2
  • 11
    • 84877722067 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 5575. For catalytic ECA leading to quaternary carbon stereogenic centers with cyanide as the nucleophilic agent, see
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 5575
  • 28
    • 79851474806 scopus 로고    scopus 로고
    • For catalytic ECA involving alkenyl-based nucleophiles and cyclic enones to afford quaternary carbon stereogenic centers, see:, T. L. May, J. A. Dabrowski, A. H. Hoveyda, J. Am. Chem. Soc. 2011, 133, 736.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 736
    • May, T.L.1    Dabrowski, J.A.2    Hoveyda, A.H.3
  • 31
    • 54249123973 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 8211; with Rh-based catalysts and sodium tetraarylborates
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 8211
  • 34
    • 77952965670 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 3969; with Rh-based catalysts and arylaluminum reagents
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 3969
  • 36
    • 78249268524 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 7769; with Pd-based catalysts and arylboronic acids
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 7769
  • 48
    • 79952543808 scopus 로고    scopus 로고
    • For application of in situ generated aryl(dialkyl)aluminum reagents in NHC-Cu-catalyzed enantioselective allylic substitution reactions, see:, F. Gao, Y. Lee, K. Mandai, A. H. Hoveyda, Angew. Chem. 2010, 122, 8548
    • (2010) Angew. Chem. , vol.122 , pp. 8548
    • Gao, F.1    Lee, Y.2    Mandai, K.3    Hoveyda, A.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.