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Volumn 69, Issue 36, 2013, Pages 7771-7778

A C-H oxidation approach for streamlining synthesis of chiral polyoxygenated motifs Dedicated to Professor Paul Wender for his pioneering and inspirational work on complexity generating organometallic reactions for streamlining complex molecule synthesis

Author keywords

Allylic alcohols; Allylic oxidation; C H oxidation; Enantioselective; Palladium; Sulfoxide

Indexed keywords

CARBON; HYDROGEN;

EID: 84880918360     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.05.012     Document Type: Article
Times cited : (24)

References (99)
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    • references therein
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    • Brubaker, J.D.1    Myers, A.G.2
  • 68
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    • 27% ee (15% yield) for octene, 40% ee (28% yield) for allylbenzene, 10 equiv starting material (SM)
    • 27% ee (15% yield) for octene, 40% ee (28% yield) for allylbenzene, 10 equiv starting material (SM): S.K. Ginotra, and V.K. Singh Tetrahedron 62 2006 3573 3581
    • (2006) Tetrahedron , vol.62 , pp. 3573-3581
    • Ginotra, S.K.1    Singh, V.K.2
  • 69
    • 0028931670 scopus 로고
    • 30% ee (50% yield) for octene, 36% ee (34% yield) for allylbenzene, 5 equiv starting material
    • 30% ee (50% yield) for octene, 36% ee (34% yield) for allylbenzene, 5 equiv starting material: M.B. Andrus, A.B. Argade, X. Chen, and M.G. Pamment Tetrahedron Lett. 36 1995 2945 2948
    • (1995) Tetrahedron Lett. , vol.36 , pp. 2945-2948
    • Andrus, M.B.1    Argade, A.B.2    Chen, X.3    Pamment, M.G.4
  • 70
    • 79959747244 scopus 로고    scopus 로고
    • 15% ee, (98% yield) 2,2-diphenylhex-5-enoic acid (1 equiv)
    • 15% ee, (98% yield) 2,2-diphenylhex-5-enoic acid (1 equiv): K. Takenaka, M. Akita, Y. Tanigaki, S. Takizawa, and H. Sasai Org. Lett. 13 2011 3506 3509
    • (2011) Org. Lett. , vol.13 , pp. 3506-3509
    • Takenaka, K.1    Akita, M.2    Tanigaki, Y.3    Takizawa, S.4    Sasai, H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.