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Volumn 13, Issue 14, 2011, Pages 3648-3651

Palladium-catalyzed oxidative rearrangement of diaryl alkenyl carbinols to β,β-diaryl α,β-unsaturated ketones

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EID: 79960174275     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol201177t     Document Type: Article
Times cited : (8)

References (27)
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    • For a review of palladium-catalyzed reactions of alcohols, see
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  • 4
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    • For reviews on palladium-catalyzed reactions proceeding through β-carboelimination
    • For reviews on palladium-catalyzed reactions proceeding through β-carboelimination, see: Seiser, T.; Cramer, N. Org. Biomol. Chem. 2009, 7, 2835
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    • Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, U.K
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    • Kuwajima, I.1    Nakamura, E.2
  • 12
    • 64549099855 scopus 로고    scopus 로고
    • For a good entry into the palladium homoenolate literature, see
    • For a good entry into the palladium homoenolate literature, see: Molander, G. A.; Jean-Gerard, L. J. Org. Chem. 2009, 74, 1297
    • (2009) J. Org. Chem. , vol.74 , pp. 1297
    • Molander, G.A.1    Jean-Gerard, L.2
  • 14
    • 67849095788 scopus 로고    scopus 로고
    • This substrate class has not been explored extensively. For the synthesis of epoxides through palladium-catalyzed carboetherification, see
    • This substrate class has not been explored extensively. For the synthesis of epoxides through palladium-catalyzed carboetherification, see: Hayashi, S; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2009, 131, 2052
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 2052
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    • For selected examples of aryl 1,2-migration in transition-metal-catalyzed reactions, see
    • For selected examples of aryl 1,2-migration in transition-metal-catalyzed reactions, see: Shen, H.-C.; Pal, S.; Lian, J.-J.; Liu, R.-S. J. Am. Chem. Soc. 2003, 125, 15762
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 15762
    • Shen, H.-C.1    Pal, S.2    Lian, J.-J.3    Liu, R.-S.4
  • 18
    • 79953219482 scopus 로고    scopus 로고
    • For a leading reference on the enantioselective hydrogenation of 1,1-diaryl alkenes, see
    • For a leading reference on the enantioselective hydrogenation of 1,1-diaryl alkenes, see: Wang, X.; Guram, A.; Caille, S.; Hu, J.; Preston, J. P.; Ronk, M.; Walker, S. Org. Lett. 2011, 13, 1881
    • (2011) Org. Lett. , vol.13 , pp. 1881
    • Wang, X.1    Guram, A.2    Caille, S.3    Hu, J.4    Preston, J.P.5    Ronk, M.6    Walker, S.7
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    • A number of benzophenones were prepared in one step from salicylaldehyde using the palladium-catalyzed cross-coupling with aryl halides. See
    • A number of benzophenones were prepared in one step from salicylaldehyde using the palladium-catalyzed cross-coupling with aryl halides. See: Satoh, T.; Itaya, T.; Miura, M.; Nomura, M. Chem. Lett. 1996, 25, 823
    • (1996) Chem. Lett. , vol.25 , pp. 823
    • Satoh, T.1    Itaya, T.2    Miura, M.3    Nomura, M.4
  • 27
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    • See Supporting Information for experimental details
    • See Supporting Information for experimental details.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.