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Volumn 74, Issue 8, 2006, Pages 680-684

One-pot vicinal and geminal double carboalkoxylation with N-carboalkoxy-imidazole by electroreduction of aromatic vinyl and imine derivatives

Author keywords

Aromatic Imine Derivatives; One Pot Geminal Carboalkoxylation; One Pot Vicinal Carboalkoxylation; Styrene Derivetices

Indexed keywords

DERIVATIVES; ELECTROCHEMISTRY; ELECTROLYTES; ESTERS; REDUCTION; STYRENE;

EID: 33749020813     PISSN: 13443542     EISSN: None     Source Type: Journal    
DOI: 10.5796/electrochemistry.74.680     Document Type: Article
Times cited : (6)

References (13)
  • 6
    • 84985611080 scopus 로고
    • In the electroreductive vicinal double C-formylation of styrene, the double C-formylated products were not isolated, but were characterized as the corresponding O-methyloxime derivatives. See Y. Engels, and H. J. Schäfer, Angew. Chem. Int. Ed. Engl., 17, 460 (1978).
    • (1978) Angew. Chem. Int. Ed. Engl. , vol.17 , pp. 460
    • Engels, Y.1    Schäfer, H.J.2
  • 12
    • 85039324517 scopus 로고    scopus 로고
    • note
    • The present elctroreductive C-carboalkoxylation of 1a using a divided cell equipped with a Pt plate as the anode, a Zn plate as the cathode and a porous ceramic filter as the diaphragm gave a complex product mixture containing less amount (Y = 20-30%) of the desired vicinal dicarboalkoxylated product (2a) accompanying some amount of tarry materials.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.