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Volumn 64, Issue 23, 2008, Pages 5435-5441

Improved preparation of alkyl 2-(3-indolyl)-3-nitroalkanoates under fully heterogeneous conditions: stereoselective synthesis of alkyl (E)-2-(3-indolyl)-2-alkenoates

Author keywords

Conjugate addition; Heterogeneous catalysis; Indoles; Nitroaldol reaction; Nitroalkenes

Indexed keywords

ACETIC ACID DERIVATIVE; ALKALOID DERIVATIVE; ALKANOIC ACID; ALKYL GROUP; CARBOLINE DERIVATIVE; ETHYL 2 OXOACETATE; INDOLE DERIVATIVE; NITROALKANE; NITROINDOLYL DERIVATIVE; NITROUS ACID; TRYPTAMINE DERIVATIVE;

EID: 43049141104     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.04.014     Document Type: Article
Times cited : (26)

References (68)
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    • For related processes using acidic activators in the reaction of indoles with methyl β-nitroacrylate see:
    • For related processes using acidic activators in the reaction of indoles with methyl β-nitroacrylate see:
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    • For a recent paper see:
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    • Ethyl acetate has been recently included among environmentally preferred solvents because of its relatively low volatility and scanty toxicity:
    • Ethyl acetate has been recently included among environmentally preferred solvents because of its relatively low volatility and scanty toxicity:
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    • For a related paper see also:
    • For a related paper see also:
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    • Review:
    • Review:
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    • For some recent examples see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.