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Volumn , Issue 20, 2010, Pages 3008-3010

Preparation of isoindolones by a lithium-iodide exchange-induced intra-molecular wurtz-fittig reaction of o -iodobenzoyl chloride/imine adducts

Author keywords

acid chloride; imines; isoindolone; metal halogen exchange; Wurtz Fittig

Indexed keywords

2 IODOBENZOYL CHLORIDE; ALKANE DERIVATIVE; CHLORIDE; IMINE; INDOLE DERIVATIVE; IODIDE; ISOINDOLONE DERIVATIVE; LITHIUM; UNCLASSIFIED DRUG;

EID: 78650172297     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1259061     Document Type: Article
Times cited : (21)

References (30)
  • 15
    • 0035680653 scopus 로고    scopus 로고
    • Enders surveys the literature by systematically considering multiple retrosynthetic disconnects for assembling isoindolones. Using his nomenclature from the aforementioned citation, Method II and Method VIII would involve the formation of a bond between the carbon to nitrogen and the ortho -C-aryl carbon (red bond designated in Scheme, structure 5).
    • Enders D, Braig V, Raabe G, Can. J. Chem. 2001 79 1528 Enders surveys the literature by systematically considering multiple retrosynthetic disconnects for assembling isoindolones. Using his nomenclature from the aforementioned citation, Method II and Method VIII would involve the formation of a bond between the carbon to nitrogen and the ortho -C-aryl carbon (red bond designated in Scheme 1, structure 5).
    • (2001) Can. J. Chem. , vol.79 , pp. 1528
    • Enders, D.1    Braig, V.2    Raabe, G.3
  • 17
    • 84981886431 scopus 로고
    • The stilbene is thought to arise from nucleophilic attack at the benzylic chloride of the acid chloride/imine adduct by another molecule of adduct which has been deprotonated at the a-chlorobenzylic position. Elimination of chloride from the resulting chloro-substituted 1,2-diphenylethane would then afford the stilbene. See
    • The stilbene is thought to arise from nucleophilic attack at the benzylic chloride of the acid chloride/imine adduct by another molecule of adduct which has been deprotonated at the a-chlorobenzylic position. Elimination of chloride from the resulting chloro-substituted 1,2-diphenylethane would then afford the stilbene. See:, Kobrich G, Angew. Chem., Int. Ed. Engl. 1972 11 473
    • (1972) Angew. Chem., Int. Ed. Engl. , vol.11 , pp. 473
    • Kobrich, G.1
  • 29
    • 78650175953 scopus 로고
    • 4), concentrated and chromatographed by flash chromatography. The isolated products were typically obtained as viscous oils
    • 19c was followed. The imines were isolated and used immediately without further purification], Stork G, Dowd S R., Org. Synth. 1974 54 46
    • (1974) Org. Synth. , vol.54 , pp. 46
    • Stork, G.1    Dowd, S.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.