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Volumn 66, Issue 34, 2010, Pages 6851-6857

One-pot synthesis of aziridines from vinyl selenones and variously functionalized primary amines

Author keywords

Aza Michael reaction; Aziridine; Ring closure; Vinyl selenone; Water

Indexed keywords

1 BENZYL 2 HEXYLAZIRIDINE; 1 BUTYL 2 HEXYLAZIRIDINE; 2 (2 PHENYL 1 AZIRIDINYL) 1 PROPANOL; 2 (2 PHENYL 1 AZIRIDINYL)ETHANOL; 2 (2 PHENYL 1 AZIRIDINYL)ETHYLAMINE; 2 HEXYL 1 [ 1 PHENYLETHYL]AZIRIDINE; 2 PHENYL 1 [ 1 PHENYLETHYL]AZIRIDINE; 4 (2 PHENYL 1 AZIRIDINYL)BUTYLAMINE; 5 (2 PHENYL 1 AZIRIDINYL) 1 PENTANOL; [ 1,2 DIPHENYL 2 (2 PHENYL 1 AZIRIDINYL) ETHYL]AMINE; [ 2 (2 PHENYLAZIRIDIN 1 YL)CYCLOHEXYL] AMINE; AMINE; AZIRIDINE DERIVATIVE; CYCLOPENT 1 ENYL PHENYL SELENONE; DIAMINE; ETHYL 3 (2 PHENYL 1 AZIRIDINYL)PROPANOATE; METHYL (2 PHENYL 1 AZIRIDINYL)ACETATE; UNCLASSIFIED DRUG; VINYL DERIVATIVE; VINYL SELENONE DERIVATIVE;

EID: 77955466442     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.06.055     Document Type: Article
Times cited : (44)

References (58)
  • 1
    • 0003535741 scopus 로고    scopus 로고
    • Organoselenium Chemistry: Modern Developments in Organic Synthesis
    • T. Wirth, Springer Berlin
    • 'Organoselenium Chemistry: Modern Developments in Organic Synthesis' T. Wirth, Top. Curr. Chem. Vol. 208 2000 Springer Berlin
    • (2000) Top. Curr. Chem. , vol.208
  • 2
    • 0003441989 scopus 로고    scopus 로고
    • Organoselenium Chemistry
    • T.G. Back, Oxford University Press Oxford, New York, NY
    • Organoselenium Chemistry T.G. Back, A Practical Approach 2000 Oxford University Press Oxford, New York, NY
    • (2000) A Practical Approach
  • 16
    • 77955467243 scopus 로고    scopus 로고
    • note
    • These papers describe cyclizations based on conjugate additions to vinyl selenones derived from nucleosides
  • 19
    • 74949098517 scopus 로고    scopus 로고
    • For general reviews on the synthesis of aziridines
    • For general reviews on the synthesis of aziridines see: H. Pellissier Tetrahedron 66 2010 1509
    • (2010) Tetrahedron , vol.66 , pp. 1509
    • Pellissier, H.1
  • 37
    • 0001842782 scopus 로고    scopus 로고
    • In the absence of 4 Å molecular sieves the aziridine 3aA was isolated in 53% yield after 32h. Molecular sieves are known to have a role as proton scavanger
    • In the absence of 4 Å molecular sieves the aziridine 3aA was isolated in 53% yield after 32h. Molecular sieves are known to have a role as proton scavanger, see: M. Terada, Y. Matsumoto, Y. Nakamura, and K. Mikami Chem. Commun. 1997 281
    • (1997) Chem. Commun. , pp. 281
    • Terada, M.1    Matsumoto, Y.2    Nakamura, Y.3    Mikami, K.4
  • 39
    • 36249014848 scopus 로고    scopus 로고
    • For some recent examples of aza-Michael additions of alkylamines to α,β-unsaturated ketones, esters, nitriles, amides and sulfones catalyzed by acids or bases
    • For some recent examples of aza-Michael additions of alkylamines to α,β-unsaturated ketones, esters, nitriles, amides and sulfones catalyzed by acids or bases see: A.P. Esteves, M.E. Silva, L.M. Rodrigues, A.M.F. Oliveira-Campos, and R. Hrdina Tetrahedron Lett. 48 2007 9040
    • (2007) Tetrahedron Lett. , vol.48 , pp. 9040
    • Esteves, A.P.1    Silva, M.E.2    Rodrigues, L.M.3    Oliveira-Campos, A.M.F.4    Hrdina, R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.