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Volumn 6, Issue 10, 1995, Pages 2527-2533

Enantioselective reaction of an imine with methyllithium catalyzed by a chiral ligand

Author keywords

[No Author keywords available]

Indexed keywords

AMINE;

EID: 0028828811     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/0957-4166(95)00331-I     Document Type: Article
Times cited : (67)

References (23)
  • 2
    • 0002991196 scopus 로고
    • Asymmetric Synthesis Utilizing External Chiral Ligands
    • (1990) Synthesis , pp. 541
    • Tomioka1
  • 15
    • 0002107234 scopus 로고
    • Control of Enantiofacial Differentiation in the Addition Reaction of Organometallics to a Nitrone in the Presence of an External Chiral Auxiliary.
    • (1993) Chemistry Letters , pp. 1313
    • Ukaji1    Hatanaka2    Ahmed3    Inomata4
  • 19
    • 84914090681 scopus 로고    scopus 로고
    • Optical antipodes of 3 and 4 gave (S)-2 in the same ees.
  • 20
    • 33751385836 scopus 로고
    • An enhancement of enantioselectivity in chiral lithium amide deprotonations due to lithium chloride
    • See, reference 3 and references cited therein. Representative LiCl effects:
    • (1993) The Journal of Organic Chemistry , vol.58 , pp. 532
    • Bunn1    Shimpkins2
  • 21
    • 84914090680 scopus 로고    scopus 로고
    • 1H-NMR spectra were taken with a JEOL GX-400 spectrometer at 400 MHz, a HITACHI R-90H spectrometer at 90 MHz. Chemical shift values are expressed in ppm relative to internal tetramethylsilane. Abbreviations are as follows: s, singlet; d, doublet; t, triplet; m, multiplet. MS were taken with a JEOL-01, SG-2 mass spectrometer or a JEOL DX-300 mass spectrometer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.