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Volumn 92, Issue 6, 1996, Pages 400-404

Synthesis of enantiomerically pure N(5)-(/-methylbenzyl-|)-aminoalcohols by regio- And stereoselective ring opening of epoxides

Author keywords

3 aminoalcohols; Chiral ligands; Enantiopure; Regioselective; Stereoselective

Indexed keywords


EID: 33749308200     PISSN: 11302283     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (16)

References (22)
  • 6
    • 33749279106 scopus 로고
    • Comprehensive Organic Synthesis
    • Trost B, Fleming I (eds) Pergamon Press. New York. Section 1.3.4.1
    • b Trost B, Fleming I (eds) (1991) Comprehensive Organic Synthesis. Selectivity, Strategy and Efficiency in Modern Organic Chemistry, Vol. 6, Pergamon Press. New York. Section 1.3.4.1. pp 88-93
    • (1991) Selectivity, Strategy and Efficiency in Modern Organic Chemistry , vol.6 , pp. 88-93
  • 13
    • 33749305138 scopus 로고    scopus 로고
    • Lithium perchloratc has been recommended as a mild and efficient catalyst in the aminolysis of epoxides
    • 9a Lithium perchloratc has been recommended as a mild and efficient catalyst in the aminolysis of epoxides:
  • 15
    • 0001797240 scopus 로고
    • Ernst B, Leumann C (eds) VCH Publishers, Basel
    • b For a recent discussion of lithium salt effects in organic synthesis, see: Seebach D, Beck KA, Studer A (1995) Modern Synthetic Methods 1995. Vol 7. Ernst B, Leumann C (eds) VCH Publishers, Basel, pp 1-178
    • (1995) Modern Synthetic Methods , vol.7 , pp. 1-178
    • Seebach, D.1    Beck, K.A.2    Studer, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.