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Volumn 77, Issue 1, 2012, Pages 525-542

An approach to the stereoselective synthesis of enantiopure dihydropyrroles and aziridines from a common sulfinyl-sulfinamide intermediate

Author keywords

[No Author keywords available]

Indexed keywords

AZIRIDINES; DIASTEREOSELECTIVE ADDITIONS; ENANTIOPURE; FUNCTIONALIZED; GOOD YIELD; PROTECTING GROUP; SIGNIFICANT IMPACTS; STEREOSELECTIVE SYNTHESIS; SULFINAMIDES; SULFINIMINES; VINYL SULFOXIDE;

EID: 84855527883     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo202144k     Document Type: Article
Times cited : (30)

References (95)
  • 34
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    • Lu, P. Tetrahedron 2010, 66, 2549-2560
    • (2010) Tetrahedron , vol.66 , pp. 2549-2560
    • Lu, P.1
  • 35
    • 1542375289 scopus 로고    scopus 로고
    • Hu, X. E. Tetrahedron 2004, 60, 2701-2743
    • (2004) Tetrahedron , vol.60 , pp. 2701-2743
    • Hu, X.E.1
  • 83
    • 3042827018 scopus 로고    scopus 로고
    • Tentative assignment for 4n′ is based on these references and on the behavior of 7l towards bromocyclization
    • García Ruano, J. L.; Alemán, J. L.; del Prado, M.; Fernández, I. J. Org. Chem. 2004, 74, 4454-4463 Tentative assignment for 4n′ is based on these references and on the behavior of 7l towards bromocyclization
    • (2004) J. Org. Chem. , vol.74 , pp. 4454-4463
    • García Ruano, J.L.1    Alemán, J.L.2    Del Prado, M.3    Fernández, I.4
  • 89
    • 77956175999 scopus 로고    scopus 로고
    • Experiments to optimize these transformations included the changing of solvents, temperature, and the presence or absence of light. 1,3-Dibromo-5,5-dimethylhydantoin as bromine source did not improve the yield of aziridine. Substitution of Ts for Ns at nitrogen did not improve the result. For a recent review on N -halo reagents, see
    • Experiments to optimize these transformations included the changing of solvents, temperature, and the presence or absence of light. 1,3-Dibromo-5,5-dimethylhydantoin as bromine source did not improve the yield of aziridine. Substitution of Ts for Ns at nitrogen did not improve the result. For a recent review on N -halo reagents, see: Veisi, H.; Ghorbani-Vaghei, R. Tetrahedron 2010, 66, 7445-7463
    • (2010) Tetrahedron , vol.66 , pp. 7445-7463
    • Veisi, H.1    Ghorbani-Vaghei, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.