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Volumn 72, Issue , 2007, Pages 633-645

Asymmetric synthesis of all stereoisomers of isofagomine using [2,3]-Wittig rearrangement

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EID: 34547851826     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-07-s(k)58     Document Type: Article
Times cited : (21)

References (50)
  • 35
    • 33845376296 scopus 로고
    • For reviews on [2,3]-Wittig rearrangement, see:
    • For reviews on [2,3]-Wittig rearrangement, see:. Nakai T., and Mikami K. Chem. Rev. 86 (1986) 885
    • (1986) Chem. Rev. , vol.86 , pp. 885
    • Nakai, T.1    Mikami, K.2
  • 36
    • 0000535071 scopus 로고
    • Trost B.M., and Fleming I. (Eds), Pergamon, Oxford
    • Marshall J.A. In: Trost B.M., and Fleming I. (Eds). Comprehensive Organic Synthesis Vol. 3 (1991), Pergamon, Oxford 975
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 975
    • Marshall, J.A.1
  • 42
    • 34547846692 scopus 로고    scopus 로고
    • N-Boc compound (R)-6 was converted to N-tosyl compound, of. which enantiomeric excess was determined by chiral HPLC (CHIRALPAK IA) to be >99%. It has been reported that reactions of cyclohexene rings proceeded with retention of stereochemistry.


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