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Volumn 18, Issue 14, 2016, Pages 3494-3497

Decarboxylative Anti-Michael Addition to Olefins Mediated by Photoredox Catalysis

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EID: 84978488781     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/acs.orglett.6b01712     Document Type: Article
Times cited : (40)

References (59)
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    • Rowlands, G. J. Tetrahedron 2009, 65, 8603 10.1016/j.tet.2009.07.001
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    • Additionally, when the photoredox coupling of 2 and trans-β-methylstyrene (8f) was run to partial conversion, recovered 8f had partially isomerized to provide a mixture of trans- and cis-β-methylstyrene, which may indicate reversible olefin addition during the reaction
    • Julia, M. Acc. Chem. Res. 1971, 4, 386 Additionally, when the photoredox coupling of 2 and trans-β-methylstyrene (8f) was run to partial conversion, recovered 8f had partially isomerized to provide a mixture of trans- and cis-β-methylstyrene, which may indicate reversible olefin addition during the reaction 10.1021/ar50047a005
    • (1971) Acc. Chem. Res. , vol.4 , pp. 386
    • Julia, M.1
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    • (Bristol-Myers Company, USA). U.S. Patent 4,800,226, January 24
    • Dillon, J. L.; Spector, R. H. (Bristol-Myers Company, USA). U.S. Patent 4,800,226, January 24, 1989.
    • (1989)
    • Dillon, J.L.1    Spector, R.H.2
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    • (Mead Johnson & Company, USA). U.S. Patent 4,394,507, July 19
    • Madding, G. D. (Mead Johnson & Company, USA). U.S. Patent 4,394,507, July 19, 1983.
    • (1983)
    • Madding, G.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.