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Volumn 18, Issue 21, 2007, Pages 2515-2530

Parallel kinetic resolution of racemic oxazolidinones using quasi-enantiomeric active esters

Author keywords

[No Author keywords available]

Indexed keywords

ESTER; OXAZOLIDINONE DERIVATIVE;

EID: 36249028791     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.10.009     Document Type: Article
Times cited : (18)

References (42)
  • 1
    • 0034599013 scopus 로고    scopus 로고
    • For parallel kinetic resolutions, see:
    • For parallel kinetic resolutions, see:. Eames J. Angew. Chem., Int. Ed. 39 (2000) 885-888
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 885-888
    • Eames, J.1
  • 8
    • 24344493479 scopus 로고    scopus 로고
    • For additional information, see Refs. 3-9
    • Zhang Q.S., and Curran D.P. Chem. Eur. J. (2005) 4866-4880 For additional information, see Refs. 3-9
    • (2005) Chem. Eur. J. , pp. 4866-4880
    • Zhang, Q.S.1    Curran, D.P.2
  • 18
    • 36248940974 scopus 로고    scopus 로고
    • For a comprehensive study into this particular active ester, see Refs. 8, 9. For further information, see: Yohannes, Y. PhD Thesis, University of London, 2004.
  • 23
    • 36249032202 scopus 로고    scopus 로고
    • The yields were based on the amount of each active ester used.
  • 24
    • 36249019499 scopus 로고    scopus 로고
    • F (light petroleum ether/diethyl ether 9:1) = 0.81 [for (R)-32], 0.69 [for (R)-14] and 0.50 [for (S)-19].
  • 25
    • 36248967854 scopus 로고    scopus 로고
    • The levels of mutual stereocontrol are quoted with respect to each parent oxazolidinone. This can potentially be interpreted as quasi-diastereoselectivity.
  • 31
    • 36248961856 scopus 로고    scopus 로고
    • Yohannes, Y. PhD Thesis, University of London, 2004.
  • 32
    • 36248994369 scopus 로고    scopus 로고
    • Dingjan, M.; Eames, J. Unpublished results.
  • 39
    • 36248955762 scopus 로고    scopus 로고
    • 3)].
  • 40
    • 36248952378 scopus 로고    scopus 로고
    • 3)].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.