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Volumn 64, Issue 41, 2008, Pages 9766-9770

Electrocatalytic cascade multicomponent assembling: stereoselective one-pot synthesis of the substituted 3-azabicyclo[3.1.0]hexane-1-carboxylate system from aldehyde, malononitrile, malonate and methanol

Author keywords

Bicyclic pyrrolidones; Cascade transformation; Electrocatalysis; Electrolysis; Mediators; Stereoselectivity

Indexed keywords

2 PYRROLIDONE DERIVATIVE; 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; 5 CYANO 4,4 DIALKOXY 2 OXO 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE DERIVATIVE; ALDEHYDE; CARBOXYLIC ACID DERIVATIVE; MALONIC ACID; MALONONITRILE; METHANOL; METHYL 5 CYANO 4,4 DIMETHOXY 2 OXO 6 PHENYL 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; METHYL 5 CYANO 4,4 DIMETHOXY 6 (2 FLUOROPHENYL) 2 OXO 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; METHYL 5 CYANO 4,4 DIMETHOXY 6 (2,4 DICHLOROPHENYL) 2 OXO 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; METHYL 5 CYANO 4,4 DIMETHOXY 6 (3 BROMOPHENYL) 2 OXO 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; METHYL 5 CYANO 4,4 DIMETHOXY 6 (3 FLUOROPHENYL) 2 OXO 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; METHYL 5 CYANO 4,4 DIMETHOXY 6 (4 CHLOROPHENYL) 2 OXO 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; METHYL 5 CYANO 4,4 DIMETHOXY 6 (4 FLUOROPHENYL) 2 OXO 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; METHYL 5 CYANO 4,4 DIMETHOXY 6 (4 METHOXYPHENYL) 2 OXO 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; METHYL 5 CYANO 4,4 DIMETHOXY 6 (4 METHYLPHENYL) 2 OXO 3 AZABICYCLO[3.1.0]HEXANE 1 CARBOXYLATE; SODIUM BROMIDE; UNCLASSIFIED DRUG;

EID: 49849106064     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.07.060     Document Type: Article
Times cited : (43)

References (29)
  • 5
    • 0003939938 scopus 로고    scopus 로고
    • For references on advanced synthetic electrochemical procedures, see:. Lund H. (Ed), Marcel Dekker, New York, NY
    • For references on advanced synthetic electrochemical procedures, see:. In: Lund H. (Ed). Organic Electrochemistry. 4th ed. (2000), Marcel Dekker, New York, NY
    • (2000) Organic Electrochemistry. 4th ed.
  • 7
    • 49849104554 scopus 로고    scopus 로고
    • For our first publication on synthetic electroorganic methodology, see:
    • For our first publication on synthetic electroorganic methodology, see:
  • 9
    • 49849092827 scopus 로고    scopus 로고
    • For recent papers, see:
    • For recent papers, see:
  • 21
    • 49849092440 scopus 로고    scopus 로고
    • Elinson, M. N., Ilovaisky, A. I.; Merkulova, V. M.; Demchuk I. V.; Belyakov, P. A.; Ogibin, Yu. N.; Nikishin G. I. Electrochim. Acta, in press. Available online 28 June 2008.
    • Elinson, M. N., Ilovaisky, A. I.; Merkulova, V. M.; Demchuk I. V.; Belyakov, P. A.; Ogibin, Yu. N.; Nikishin G. I. Electrochim. Acta, in press. Available online 28 June 2008.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.