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Volumn 72, Issue 2, 2007, Pages 431-434

Single enantiomer epoxides by bromomandelation of prochiral alkenes

Author keywords

[No Author keywords available]

Indexed keywords

BROMOMANDELATION; CYCLOHEXENES; ENANTIOMER EPOXIDES;

EID: 33846256722     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo061818r     Document Type: Article
Times cited : (17)

References (20)
  • 5
    • 1042265088 scopus 로고    scopus 로고
    • For leading references to the catalytic kinetic enantioselective opening of terminal epoxides, see: a
    • For leading references to the catalytic kinetic enantioselective opening of terminal epoxides, see: (a) Nielsen, L. P. C.; Stevenson, C. P.; Blackmond, D. G.; Jacobsen, E. N. J. Am. Chem. Soc. 2004, 126, 1360.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 1360
    • Nielsen, L.P.C.1    Stevenson, C.P.2    Blackmond, D.G.3    Jacobsen, E.N.4
  • 7
    • 0000931779 scopus 로고    scopus 로고
    • For leading references to the catalytic enantioselective opening of cyclohexene epoxide, see: a
    • For leading references to the catalytic enantioselective opening of cyclohexene epoxide, see: (a) McCleland, B. W.; Nugent, W. A.; Finn, M. G. J. Org. Chem. 1998, 63, 6656.
    • (1998) J. Org. Chem , vol.63 , pp. 6656
    • McCleland, B.W.1    Nugent, W.A.2    Finn, M.G.3
  • 11
    • 0000033850 scopus 로고
    • For the use of O-methyl mandelate esters to resolve preformed halohydrins, see
    • (b) For the use of O-methyl mandelate esters to resolve preformed halohydrins, see: Konopelski, J. P.; Boehler, M. A.; Tarasow, T. M. J. Org. Chem. 1989, 54, 4966.
    • (1989) J. Org. Chem , vol.54 , pp. 4966
    • Konopelski, J.P.1    Boehler, M.A.2    Tarasow, T.M.3
  • 13
    • 0026074793 scopus 로고
    • For bromoacetoxylation of a terminal alkene, see
    • (a) For bromoacetoxylation of a terminal alkene, see: Srikrishna, A.; Sundarababu, G. Tetrahedron 1991, 47, 481.
    • (1991) Tetrahedron , vol.47 , pp. 481
    • Srikrishna, A.1    Sundarababu, G.2
  • 14
    • 7144242358 scopus 로고
    • For bromoacetoxylation of cyclohexene, see
    • (b) For bromoacetoxylation of cyclohexene, see: Dulcère, J. P.; Rodríguez, J. Synlett 1992, 347.
    • (1992) Synlett , pp. 347
    • Dulcère, J.P.1    Rodríguez, J.2
  • 20
    • 33645036043 scopus 로고    scopus 로고
    • For the use of an enantiomerically pure cis-2-aminocyclohexanol as an effective ligand for the enantioselective reduction of a ketone, see
    • For the use of an enantiomerically pure cis-2-aminocyclohexanol as an effective ligand for the enantioselective reduction of a ketone, see: Schiffers, I.; Rantanen, T.; Schmidt, F.; Bergmans, W.; Zani, L.; Bolm, C. J. Org. Chem. 2006, 71, 2320.
    • (2006) J. Org. Chem , vol.71 , pp. 2320
    • Schiffers, I.1    Rantanen, T.2    Schmidt, F.3    Bergmans, W.4    Zani, L.5    Bolm, C.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.