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Volumn 8, Issue 11, 2006, Pages 960-96

A green route to β-amino alcohols via the uncatalyzed aminolysis of 1,2-epoxides by alkyl- and arylamines

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EID: 33750466153     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/b607620c     Document Type: Article
Times cited : (62)

References (46)
  • 3
    • 0004252595 scopus 로고    scopus 로고
    • P. A. Grieco, Blackie Academic and Professional, London
    • Organic Synthesis in Water, ed. P. A. Grieco, Blackie Academic and Professional, London, 1998.
    • (1998) Organic Synthesis in Water
  • 6
    • 24044470646 scopus 로고    scopus 로고
    • C. J. Li Chem. Rev. 2005 105 3095-3165.
    • (2005) Chem. Rev. , vol.105 , pp. 3095-3165
    • Li, C.J.1
  • 46
    • 0033529831 scopus 로고    scopus 로고
    • At pH 4.2 the azidolysis of 1,2-epoxides is strongly catalyzed and generally gives a C-α regioselectivity, indicating that the process proceeds on the protonated oxirane-ring
    • At pH 4.2 the azidolysis of 1,2-epoxides is strongly catalyzed and generally gives a C-α regioselectivity, indicating that the process proceeds on the protonated oxirane-ring: F. Fringuelli F. Pizzo L. Vaccaro J. Org. Chem. 1999 64 6094-6096.
    • (1999) J. Org. Chem. , vol.64 , pp. 6094-6096
    • Fringuelli, F.1    Pizzo, F.2    Vaccaro, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.