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Volumn 47, Issue 34, 2008, Pages 6367-6370

Palladium-catalyzed enantioselective oxidation of chiral secondary alcohols: Access to both enantiomeric series

Author keywords

Alcohols; Asymmetric catalysis; Oxidation; Palladium; Synthetic methods

Indexed keywords

CHEMICAL REACTIONS; PALLADIUM;

EID: 52049096917     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200801865     Document Type: Article
Times cited : (68)

References (31)
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  • 8
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    • Simultaneous with our report, a similar system was reported, see
    • Simultaneous with our report, a similar system was reported, see: D. R. Jensen, J. S. Pugsley, M. S. Sigman, J. Am. Chem. Soc. 2001, 123, 7475-7476.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 7475-7476
    • Jensen, D.R.1    Pugsley, J.S.2    Sigman, M.S.3
  • 11
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    • For discussions of kinetic resolution, see: a, Ed, E. L. Eliel, Wiley, New York
    • For discussions of kinetic resolution, see: a) H. B. Kagan, J. C. Fiaud in Topics in Stereochemistry, Vol. 18 (Ed.: E. L. Eliel), Wiley, New York, 1988, pp. 249-330;
    • (1988) Topics in Stereochemistry , vol.18 , pp. 249-330
    • Kagan, H.B.1    Fiaud, J.C.2
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    • 21344465658 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3974-4001.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 3974-4001
  • 15
    • 0037986275 scopus 로고    scopus 로고
    • For examples with alternative ligands in the palladium-catalyzed oxidative kinetic resolution of secondary alcohols, see: a D. R. Jensen, M. S. Sigman, Org. Lett. 2003, 5, 63-65;
    • For examples with alternative ligands in the palladium-catalyzed oxidative kinetic resolution of secondary alcohols, see: a) D. R. Jensen, M. S. Sigman, Org. Lett. 2003, 5, 63-65;
  • 19
    • 53349158615 scopus 로고    scopus 로고
    • See the Supporting Information for details
    • See the Supporting Information for details.
  • 20
    • 53349110892 scopus 로고    scopus 로고
    • 3> I> OAc, see the Supporting Information for details.
    • 3> I> OAc, see the Supporting Information for details.
  • 22
  • 23
    • 53349169585 scopus 로고    scopus 로고
    • 2] as the catalyst, see the Supporting Information for details.
    • 2] as the catalyst, see the Supporting Information for details.
  • 24
    • 53349105372 scopus 로고    scopus 로고
    • slow = ln[(1-C)(1-ee)]/ln[(1- C)(1+ee)], where C is conversion, see: reference [6a].
    • slow = ln[(1-C)(1-ee)]/ln[(1- C)(1+ee)], where C is conversion, see: reference [6a].
  • 25
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    • 2 sources, see the Supporting Information for details.
    • 2 sources, see the Supporting Information for details.
  • 26
    • 0001147659 scopus 로고    scopus 로고
    • For an asymmetric synthesis of, -sparteine, see
    • For an asymmetric synthesis of (+)-sparteine, see: B. T. Smith, J. A. Wendt, J. Aubé, Org. Lett. 2002, 4, 2577-2579.
    • (2002) Org. Lett , vol.4 , pp. 2577-2579
    • Smith, B.T.1    Wendt, J.A.2    Aubé, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.