메뉴 건너뛰기




Volumn 46, Issue 44, 2005, Pages 7487-7490

An efficient and facile one-pot synthesis of cyanohydrin esters from carbonyl compounds catalyzed by iron(III) chloride

Author keywords

Acid anhydride; Carbonyl compound; Cyanation; Cyanohydrin ester; Iron(III) chloride; Trimethylsilyl cyanide

Indexed keywords

ACID ANHYDRIDE; CARBONYL DERIVATIVE; CYANIDE; CYANOHYDRIN; ESTER; FERROUS CHLORIDE;

EID: 26244466243     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.09.003     Document Type: Article
Times cited : (38)

References (41)
  • 19
    • 0037010804 scopus 로고    scopus 로고
    • Other iron(III) chloride-catalyzed useful reactions of silyl-substituted nucleophiles: T. Watahiki, and T. Oriyama Tetrahedron Lett. 43 2002 8959
    • (2002) Tetrahedron Lett. , vol.43 , pp. 8959
    • Watahiki, T.1    Oriyama, T.2
  • 36
    • 84985616518 scopus 로고
    • Acyl cyanide can be synthesized from the corresponding acid halide with metal cyanide or trimethylsilyl cyanide: K. Haase, and H.M.R. Hoffmann Angew. Chem., Int. Ed. Engl. 21 1982 83
    • (1982) Angew. Chem., Int. Ed. Engl. , vol.21 , pp. 83
    • Haase, K.1    Hoffmann, H.M.R.2
  • 39
    • 26244438211 scopus 로고    scopus 로고
    • note
    • 4. α-(Acetoxy)phenylacetonitrile (48.7 mg, 94%) was isolated by thin-layer chromatography on silica gel.
  • 40
    • 26244462670 scopus 로고    scopus 로고
    • note
    • 1H NMR analysis (400 MHz) using 1,1,2,2-tetrachloroethane as an internal standard.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.