Studies on Thiophene Derivatives. IV. Syntheses of 2-Aminoethyl 3, 3-Diaryl-3-hydroxypropanoates and 3, 3-Diaryl-2-prpenoates.
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چکیده
منابع مشابه
Synthesis of 1, 3-diaryl Substituted Iodobenzene Derivatives
The synthesis and characterization a new derivatives of 2'-iodo-meta terphenyl from the reaction ofexcess aryl-Grignard and 2, 6- dichloroiodobenzene with quenching of m-terphenyl-2'-magnesiumbromide by iodine is reported. Via the reactions three carbon-carbon bonds are constructed and mterphenylsare obtained in good yields.
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A synthesis of 2-Isonicotinyl 3, 5-diaryl -2H-(3-tetrazolium) chloride (5) was performed starting from isonicotinic hydrazide (1). The treatment of 1 with various substituted aromatic aldehydes afforded the corresponding Schiff’s bases 3. The Schiff’s bases are converted into a series of aryl formazan via diazocoupling which underwent cyclization in the presence of H2O2 and KMnO4 to give substi...
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the synthesis and characterization a new derivatives of 2'-iodo-meta terphenyl from the reaction ofexcess aryl-grignard and 2, 6- dichloroiodobenzene with quenching of m-terphenyl-2'-magnesiumbromide by iodine is reported. via the reactions three carbon-carbon bonds are constructed and mterphenylsare obtained in good yields.
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3-(2-Furanyl)-2-propenoic acid has been used to prepare a new series of organotin complexes of general formula R3SnL (R=Me, Et, n-Bu, Ph and Cy) and R2SnL2 (R=Me and n-Bu). These complexes have been characterized by elemental analyses, IR, 1H-NMR, MASS and Mössbaure spectroscopy.
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An efficient synthesis of some novel coumarin derivatives via 1, 4- Michael addition of indole to coumarin chalcones catalyzed by cellulose sulphonic acid (CSA) under solvent free conditions is described. The corresponding Michael addition products were obtained in good to excellent yield. The synthesized compounds were screened for their antibacterial activity against E. coli, S. aureus and an...
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ژورنال
عنوان ژورنال: Chemical and Pharmaceutical Bulletin
سال: 1960
ISSN: 0009-2363,1347-5223
DOI: 10.1248/cpb.8.103