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Volumn 15, Issue 4, 2013, Pages 852-855

N-bromosuccinimide/1,8-diazabicyclo[5.4.1]undec-7-ene combination: β-amination of chalcones via a tandem bromoamination/debromination sequence

Author keywords

[No Author keywords available]

Indexed keywords

BROMINATED HYDROCARBON; CHALCONE DERIVATIVE; FUSED HETEROCYCLIC RINGS; N BROMOSUCCINIMIDE;

EID: 84873964645     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol303539u     Document Type: Article
Times cited : (47)

References (44)
  • 24
    • 84863469502 scopus 로고    scopus 로고
    • Generally, the reaction of α,β-unsaturated enones with NBS gave haloaminated products under acidic conditions, most often with external amino sources. Examples with the imido moiety from NBS itself are rare. For such a recent example of vicinal haloimination of enecarbamates with NBS catalyzed by phosphate salt, see: Alix, A.; Lalli, C.; Retailleau, P.; Masson, G. J. Am. Chem. Soc. 2012, 134, 10389
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 10389
    • Alix, A.1    Lalli, C.2    Retailleau, P.3    Masson, G.4
  • 29
    • 84873941038 scopus 로고    scopus 로고
    • CCDC 879831 (2f) contains the supplementary crystallographic data for this paper. The data can be obtained free of charge from The Cambridge Crystallographic Data Centre via. See the Supporting Information.
    • CCDC 879831 (2f) contains the supplementary crystallographic data for this paper. The data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif. See the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.