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Volumn , Issue 20, 2006, Pages 3533-3539

Oxidative kinetic resolution-Claisen rearrangement sequence to enantioenriched arylcycloalkenes

Author keywords

Claisen rearrangement; Oxidative cyclization; Oxidative kinetic resolution; Palladium catalysis; Secondary alcohols

Indexed keywords

ALKENE DERIVATIVE; ALLYL ALCOHOL; ARYLCYCLOALKENE DERIVATIVE; LEWIS ACID; PALLADIUM; TERTIARY ALKYL GROUP; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 33846543786     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-958415     Document Type: Article
Times cited : (14)

References (27)
  • 1
    • 0034794864 scopus 로고    scopus 로고
    • For oxidative kinetic resolutions, see: a
    • For oxidative kinetic resolutions, see: (a) Ferreira, E. M.; Stoltz, B. M. J. Am. Chem. Soc. 2001, 123, 7725.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 7725
    • Ferreira, E.M.1    Stoltz, B.M.2
  • 5
    • 3042643476 scopus 로고    scopus 로고
    • Nielson, R. J.; Keith, J. M.; Stoltz, B. M.; Goddard, W. A. III J. Am. Chem. Soc. 2004, 126, 7967.
    • (e) Nielson, R. J.; Keith, J. M.; Stoltz, B. M.; Goddard, W. A. III J. Am. Chem. Soc. 2004, 126, 7967.
  • 10
    • 0034823071 scopus 로고    scopus 로고
    • Simultaneous to our publication, a related system was reported, see: a
    • Simultaneous to our publication, a related system was reported, see: (a) Jensen, D. R.; Pugsley, J. S.; Sigman, M. S. J. Am. Chem. Soc. 2001, 123, 7475.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 7475
    • Jensen, D.R.1    Pugsley, J.S.2    Sigman, M.S.3
  • 18
    • 33748480130 scopus 로고    scopus 로고
    • For application to natural product synthesis, see
    • For application to natural product synthesis, see: Tambar, U. K.; Ebner, D. C.; Stoltz, B. M. J. Am. Chem. Soc. 2006, 128, 11752.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 11752
    • Tambar, U.K.1    Ebner, D.C.2    Stoltz, B.M.3
  • 19
    • 1942535137 scopus 로고    scopus 로고
    • For application to the synthesis of pharmaceutical intermediates, see
    • For application to the synthesis of pharmaceutical intermediates, see: Caspi, D. D.; Ebner, D. C.; Bagdanoff, J. T.; Stoltz, B. M. Adv. Synth. Catal. 2004, 346, 185.
    • (2004) Adv. Synth. Catal , vol.346 , pp. 185
    • Caspi, D.D.1    Ebner, D.C.2    Bagdanoff, J.T.3    Stoltz, B.M.4
  • 26
    • 33846468792 scopus 로고    scopus 로고
    • The decreased ee for this substrate is presumably due to competing 1,3-rearrangement, leading to partial racemization
    • The decreased ee for this substrate is presumably due to competing 1,3-rearrangement, leading to partial racemization.
  • 27
    • 33846494939 scopus 로고    scopus 로고
    • note


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.