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Volumn , Issue 11, 1998, Pages 2397-2403

Enantioselective lithiation and substitution of (E)-cinnamyl N,N-diisopropylcarbamate through use of (-)-sparteine complexes

Author keywords

( ) Sparteine; Asymmetric synthesis; Chiral allylic anions; Enantioselective deprotonation; Stereochemistry of electrophilic allylic substitution

Indexed keywords


EID: 2842586098     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(199811)1998:11<2397::aid-ejoc2397>3.0.co;2-2     Document Type: Article
Times cited : (49)

References (44)
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    • note
    • -3, Flack parameter O 07(4), hydrogens calculated and refined as riding atoms. The data set was collected with an Enraf-Nonius MACH3 diffractometer. Programs used: data reduction: MolEN, structure solution: SHELXS-86, structure refinement: SHELXL-93, graphics: SCHAKAL-92. Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-100987. Copies of the data can be obtained free of charge on application to The Director, CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK [Fax: (internat.) +44 (0)1223 336033, e-mail: deposit@ccdc.cam.ac.uk].
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    • Melting point of the racemic compound
    • Melting point of the racemic compound.
  • 41
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    • Signal appears at lower field
    • Signal appears at lower field.
  • 42
    • 2842571042 scopus 로고    scopus 로고
    • The enantiomeric excess was deduced from the hydrogenation experiment
    • The enantiomeric excess was deduced from the hydrogenation experiment.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.