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Volumn , Issue 4, 1998, Pages 729-733

Diastereo- and Enantioselective Synthesis of (+)- and (-)-cis-2-Aminocyclobutanols

Author keywords

Asymmetric synthesis; Hydrogenation; Hydrogenolysis; Amino alcohols

Indexed keywords


EID: 0002960798     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(199804)1998:4<729::aid-ejoc729>3.0.co;2-b     Document Type: Article
Times cited : (35)

References (22)
  • 1
    • 0004255370 scopus 로고
    • University Press, Cambridge, and references cited therein
    • R. A. Aitken, S. N. Kilényi, Asymmetric Synthesis, University Press, Cambridge, 1992, 83-142, and references cited therein.
    • (1992) Asymmetric Synthesis , pp. 83-142
    • Aitken, R.A.1    Kilényi, S.N.2
  • 6
    • 84985656340 scopus 로고
    • [3d] For the influence of the reducing agent and the catalyst on the diastereo- and enantioselectivity see: G. Knupp, A. W. Frahm, Arch. Pharm. 1985. 318, 250-257.
    • (1985) Arch. Pharm. , vol.318 , pp. 250-257
    • Knupp, G.1    Frahm, A.W.2
  • 16
    • 2742574162 scopus 로고    scopus 로고
    • note
    • 1H-NMR spectroscopy. We assume that these structures are the result of a non-stereoselective 1,2-rearrangement, probably via an enamine intermediate, which is currently being investigated.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.