Regioselective synthesis of novel ketene dithioacetals
作者: Azizollah HabibiYousef ValizadehAbdolali AlizadehHadi Amiri RudbariViviana Mollica Nardo
作者单位: 1Faculty of Chemistry , Kharazmi (Tarbiat Moallem) University , No. 43, Mofateh Avenue, Tehran , Iran
2Department of Chemistry , Tarbiat Modares University , PO Box 14115-175, Tehran , Iran
3Faculty of Chemistry , University of Isfahan , 81746-73441 , Isfahan , Iran
4Università degli Studi di Messina , dip. Scienze Chimiche, Viale Ferdinando S. d'Alcontres, 98166 Messina , Italy
刊名: Journal of Sulfur Chemistry, 2014, Vol.35 (4), pp.362-372
来源数据库: Taylor & Francis Journal
DOI: 10.1080/17415993.2013.879871
关键词: ketene dithioacetalactive methylene compoundsdialkyl acetylenedicarboxylate5- endo-trig cyclizationMichael addition
原始语种摘要: A series of novel ketene dithioacetals has been synthesized by condensation of active methylene compounds with carbon disulfide in the presence of dialkyl acetylenedicarboxylates. This regioselective reaction provides products in good yield by a Michael addition reaction followed by 5-endo-trig intramolecular cyclization. Structures of synthesized compounds have been characterized by elemental analysis, FT-IR, 1H NMR, 13C NMR, and mass spectra. The crystal structure of compound (C 17H 22O 6S 2) has been determined.
全文获取路径: Taylor & Francis  (合作)
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影响因子:1.101 (2012)

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