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Volumn 15, Issue 12, 2009, Pages 2966-2978

Selectively N-protected enantiopure 2,5-disubstituted piperazines: Avoiding the pitfalls in solid-phase Fukuyama-Mitsunobu cyclizations

Author keywords

Aminolysis; Aziridines; Fukuyama Mitsunobu cyclization; Piperazines; Solid phase synthesis

Indexed keywords

ALDEHYDES; AMINATION; AMINES; AMINO ACIDS; AROMATIC HYDROCARBONS; CHEMICAL COMPOUNDS; GROUP TECHNOLOGY; METHANOL; MICROWAVES; ORGANIC ACIDS; RESINS; SYNTHESIS (CHEMICAL); UREA;

EID: 62349101581     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200802044     Document Type: Article
Times cited : (20)

References (56)
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    • 0037668345 scopus 로고    scopus 로고
    • For selected examples in solution, see: a
    • For selected examples in solution, see: a) W. Kurosawa, T. Kan, T. Fukuyama, J. Am. Chem. Soc. 2003, 125, 8112-8113;
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 8112-8113
    • Kurosawa, W.1    Kan, T.2    Fukuyama, T.3
  • 39
    • 0027214104 scopus 로고    scopus 로고
    • (S)-(1-Tritylaziridin-2-yl)methanol was synthesized according to a procedure described by I. Utsunomiya, M. Fuji, T Sato, M. Natsume, Chem. Pharm. Bull. 1993, 41, 854-860.
    • (S)-(1-Tritylaziridin-2-yl)methanol was synthesized according to a procedure described by I. Utsunomiya, M. Fuji, T Sato, M. Natsume, Chem. Pharm. Bull. 1993, 41, 854-860.
  • 47
    • 0030790051 scopus 로고    scopus 로고
    • Previously, nitrobenzenesulfonyl-activated aziridines have been successfully subjected to ring-opening with amine nucleophiles in solution. See: a
    • Previously, nitrobenzenesulfonyl-activated aziridines have been successfully subjected to ring-opening with amine nucleophiles in solution. See: a) P. E. Maligres, M. M. See, D. Askin, P. J. Reider, Tetrahedron Lett. 1997, 38, 5253-5256;
    • (1997) Tetrahedron Lett , vol.38 , pp. 5253-5256
    • Maligres, P.E.1    See, M.M.2    Askin, D.3    Reider, P.J.4
  • 52
    • 62349108753 scopus 로고    scopus 로고
    • For the synthesis of allyl 2,4-dinitrophenyl. carbonate see Experimental. Section.
    • For the synthesis of allyl 2,4-dinitrophenyl. carbonate see Experimental. Section.
  • 56
    • 0037424873 scopus 로고    scopus 로고
    • Methyl (S)-1-tritylaziridine-2-carboxylate was synthesized according to a procedure, described by B. McKeever, G. Pattenden, Tetrahedron 2003, 59, 2701-2712.
    • Methyl (S)-1-tritylaziridine-2-carboxylate was synthesized according to a procedure, described by B. McKeever, G. Pattenden, Tetrahedron 2003, 59, 2701-2712.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.