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Volumn 12, Issue 8, 2010, Pages 1752-1755

Highly endo -selective and enantioselective 1,3-dipolar cycloaddition of azomethine ylide with α-enones catalyzed by a silver(I)/thioclickferrophos complex

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EID: 77951165292     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol100336q     Document Type: Article
Times cited : (135)

References (58)
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    • For examples
    • For examples
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    • For reviews, see
    • For reviews, see
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    • For reviews, see
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  • 11
    • 77950244957 scopus 로고    scopus 로고
    • 1,3-dipolar cycloaddition.
    • Ma S., Ed.; Wiley-VCH: Weinheim, Germany
    • Hashimoto, T.; Maruoka, K. 1,3-Dipolar Cycloaddition. In Handbook of Cyclization Reactions; Ma, S., Ed.; Wiley-VCH: Weinheim, Germany, 2010; Vol. 1, pp 87 - 168.
    • (2010) Handbook of Cyclization Reactions , vol.1 , pp. 87-168
    • Hashimoto, T.1    Maruoka, K.2
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    • For selected recent examples, see
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    • For selected recent examples, see
    • For selected recent examples, see
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    • 0345731484 scopus 로고    scopus 로고
    • The diastereoselective reaction with chiral 2-sulfinyl 2-cyclopentenone has been reported
    • The diastereoselective reaction with chiral 2-sulfinyl 2-cyclopentenone has been reported: Ruano, J. L. G.; Tito, A.; Peromingo, M. T. J. Org. Chem. 2003, 68, 10013-10019
    • (2003) J. Org. Chem. , vol.68 , pp. 10013-10019
    • Ruano, J.L.G.1    Tito, A.2    Peromingo, M.T.3
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    • For recent reviews for chiral ferrocenyl phosphines, see
    • For recent reviews for chiral ferrocenyl phosphines, see
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    • For an example of chiral ferrocenyl P, S -ligand other than FeSulphos in asymmetric 1,3-dipolar addition with azomethine ylides, see
    • For an example of chiral ferrocenyl P, S -ligand other than FeSulphos in asymmetric 1,3-dipolar addition with azomethine ylides, see
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    • X-ray crystallographic structure of AgOAc/ L5 complex was obtained. The crystallographic coordinates have been deposited with the Cambridge Crystallographic Data Centre; deposition no. 704687. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre, 12 Union Rd., Cambridge CB2 1EZ, UK or via www.ccdc.cam.ac.uk/conts/retrieving.html.
    • X-ray crystallographic structure of AgOAc/ L5 complex was obtained. The crystallographic coordinates have been deposited with the Cambridge Crystallographic Data Centre; deposition no. 704687. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre, 12 Union Rd., Cambridge CB2 1EZ, UK or via www.ccdc.cam.ac.uk/conts/retrieving.html.
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    • The reaction with a vinyl kenone such as 1-phenyl-2-propen-1-one was also examined (Supporting Information).
    • The reaction with a vinyl kenone such as 1-phenyl-2-propen-1-one was also examined (Supporting Information).


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