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Volumn 8, Issue 2, 2006, Pages 349-351

Synthesis of enantiopure allylamines by reductive alkylation of amino epoxides with organolithium reagents

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EID: 31544478243     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0529602     Document Type: Article
Times cited : (18)

References (51)
  • 33
    • 0000763561 scopus 로고    scopus 로고
    • To see two reviews of olefination of α-aminoaldehydes: (a) Reetz, M. T. Chem. Rev. 1999, 99, 1121-1162.
    • (1999) Chem. Rev. , vol.99 , pp. 1121-1162
    • Reetz, M.T.1
  • 35
    • 85004872164 scopus 로고
    • α-Amino aldehydes are often susceptible to racemization: (a) Fehrentz, J. A.; Castro, B. Synthesis 1983, 676-678.
    • (1983) Synthesis , pp. 676-678
    • Fehrentz, J.A.1    Castro, B.2
  • 41
    • 0001318042 scopus 로고    scopus 로고
    • Reviews: (a) Satoh, T. Chem. Rev. 1996, 96, 3303-3325.
    • (1996) Chem. Rev. , vol.96 , pp. 3303-3325
    • Satoh, T.1
  • 49
    • 31544445039 scopus 로고    scopus 로고
    • note
    • 4, filtered, and concentrated in vacuo. Flash column chromatography on silica gel (hexane/EtOAc 10:1) provided pure compounds 2.
  • 51
    • 31544461570 scopus 로고    scopus 로고
    • note
    • Chiracel OD, UV detector 210 nm, 0.5 mL/min, hexane, rt: 2h 18.826 min; rt: enantiomer of 2h 13.737 min.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.