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Volumn 60, Issue 21, 1995, Pages 6696-6699

Highly Diastereoselective Synthesis of Threo or Erythro Aminoalkyl Epoxides from α-Amino Acids

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EID: 0001430378     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00126a019     Document Type: Article
Times cited : (104)

References (30)
  • 17
    • 0027515031 scopus 로고
    • Threo peptidyl epoxides have been synthesized from peptidyl olefins with high steroseleclectivity
    • Threo peptidyl epoxides have been synthesized from peptidyl olefins with high steroseleclectivity: Romeo, S.; Rich, D. H. Tetrahedron Lett. 1993, 34, 7187.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 7187
    • Romeo, S.1    Rich, D.H.2
  • 25
    • 0001244705 scopus 로고
    • Other synthetic method to prepare chloromethyl ketones employing the mixed anhydride-diazomethyl ketone route
    • Other synthetic method to prepare chloromethyl ketones employing the mixed anhydride-diazomethyl ketone route: Schoellmann, G.; Shaw, E. Biochemistry 1963, 2, 252.
    • (1963) Biochemistry , vol.2 , pp. 252
    • Schoellmann, G.1    Shaw, E.2
  • 27
    • 0027308188 scopus 로고
    • A related intermediated was recently isolated by silylation as the corresponding monosilylketal derivative
    • A related intermediated was recently isolated by silylation as the corresponding monosilylketal derivative: Barluenga, J.; Pedregal, B.; Concellón, J. M. Tetrahedron Lett. 1993, 31, 4563.
    • (1993) Tetrahedron Lett. , vol.31 , pp. 4563
    • Barluenga, J.1    Pedregal, B.2    Concellón, J.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.