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Volumn 46, Issue 19, 2005, Pages 3279-3282

Highly efficient KF/Al2O3-catalyzed versatile hetero-Michael addition of nitrogen, oxygen, and sulfur nucleophiles to α,β-ethylenic compounds

Author keywords

Heteroatom; Lewis base; Michael reaction; Nitrogen; Oxygen

Indexed keywords

ETHYLENE DERIVATIVE; NITROGEN; OXYGEN; SULFUR;

EID: 17144364630     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.03.112     Document Type: Article
Times cited : (105)

References (37)
  • 30
    • 85030796383 scopus 로고    scopus 로고
    • note
    • 4, concentrated to give the crude product, and then purified by silica column chromatography to afford pure product. (eluting solvent: EtOAc-petroleum ether). Method B: it is different in workup. After the mixture was stirring for given time, the catalyst was removed by simple filtration. The solvent was evaporated to give the crude and then purified by silica column chromatography to afford pure product
  • 31
    • 0003405157 scopus 로고
    • Georg Thieme Stuttgart
    • Although there is no report in the literature about the conversion of these product in this aza-Michael reaction, the functional moiety can undergo further conversions using well-established procedure group chemistry P.J. Kocienski Protecting Groups 1994 Georg Thieme Stuttgart p 195
    • (1994) Protecting Groups
    • Kocienski, P.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.