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Volumn , Issue 7, 1998, Pages 733-734

Addition of allylmagnesium bromide to ROPHy/SOPHy aldoximes: Asymmetric synthesis of protected β-amino acids

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EID: 0002691294     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-1767     Document Type: Article
Times cited : (13)

References (36)
  • 2
    • 0028130028 scopus 로고
    • For reviews on the asymmetric synthesis of β-amino acids, see: Cole, D. C. Tetrahedron 1994, 50, 9517;
    • (1994) Tetrahedron , vol.50 , pp. 9517
    • Cole, D.C.1
  • 20
    • 0029959913 scopus 로고    scopus 로고
    • For other recent approaches, see ref. 2, and the following: Seki, M.; Matsumoto, K. Tetrahedron Lett. 1996, 37, 3165;
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3165
    • Seki, M.1    Matsumoto, K.2
  • 30
    • 26844491170 scopus 로고    scopus 로고
    • note
    • 3), filtered and evaporated. The residue was purified by flash chromatography on silica gel using dichloromethane-light petroleum (1:2) as eluent to give the hydroxylamine 2.
  • 32
    • 26844515495 scopus 로고    scopus 로고
    • note
    • The N-O bond cleavage and N-protection steps were carried out exactly as described in ref. 9.
  • 33
    • 26844468753 scopus 로고    scopus 로고
    • note
    • 3).
  • 35
    • 26844453954 scopus 로고    scopus 로고
    • note
    • 4)), filtered and evaporated. Column chromatography on silica gel eluting with ether-light petroleum (1:1) gave the amino ester 4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.