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Katritzky, Academic Press, Inc. Detty and B. Murray, J. Detty, J. McKelvey and H. Nivorozhkin and I. Sadekov, Khim. Detty and H. Sadekov, A. Ladatko, E. Sadekova, G. Dorofeenko and V. Minkin, Khim. Sashida, H. Kurahashi and T. Tsuchiya, J. Sashida, K. Ito and T. Tsuchiya, Chem.

Sadamori and T.

Tsuchiya, Synth. Sashida and A. Kawamukai, J. Molecules, 7, Medicinal Chemistry Research, 21, Der Pharma Chemica, 4, Molecules, 18, United Arab Republic Journal of Chemistry, 13, Indian Journal of Chemistry, 44B, Ultrasonics Sonochemistry, 16, Molecules, 16, Der Pharma Chemica, 3, Journal of the Serbian Chemical Society, 71, Journal of King Saud University-Science, 19, Journal of the Serbian Chemical Society, 77, Rasayan Journal of Chemistry, 3, Tetrahedron, 32, Journal of Chemical Education, 64, Indian Journal of Chemistry, 48B, The Journal of Organic Chemistry, 52, Synthetic Communications, 33, Synthetic Communications, 32, Green Chemistry, 5, Synthesis, , Catalysis Communications, 8, European Journal of Medicinal Chemistry, 44, E-Journal of Chemistry, 9, Molecules, 17, Der Chemica Sinica, 3, Physical Chemistry Chemical Physics, 14, Journal of the American Chemical Society, 75, Indian Journal of Chemistry, 52B, Journal of the American Chemical Society, 78, One-Pot Synthesis of Flavonols.

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Journal of Heterocyclic Chemistry, 24, Tetrahedron, 19, The Journal of Organic Chemistry, 65, Berichte der deutschen chemischen Gesellschaft, 41, Part Journal of Medicinal Chemistry, 54, Tetrahedron Letters, 4, Chemische Berichte, 97, Indian Journal of Chemistry, 45B, Chemical Communications, 3, Bulletin of the Chemical Society of Japan, 65, Tetrahedron, 61, Tetrahedron Letters, 49, Phytochemistry, 55, Maximizing the Antioxidant Activity of Phenols. Journal of the American Chemical Society, , Journal of Heterocyclic Chemistry, 45, Part I.

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nomenclature of heterocyclic compounds

IV, 2nd Edition, Part XI. Stereochemistry of the Products. Nature and Science, 8, Tetrahedron Letters, 43, Molecules, 15, University of Gottingen, Gottingen. Organic Letters, 6, Chinese Journal of Structurnal Chemistry, 30, Tetrahedron Letters, 46, OEt2-Catalyzed Knoevenagel condensation. Bulletin of the Korean Chemical Society, 31, Journal of the Korean Chemical Society, 55, Synthetic Communications, 27, Heterocycles, 20, Chinese Chemical Letters, 14, Journal of the Chinese Chemical Society, 51, Advances in Heterocyclic Chemistry, 38, Iridoids, Tetrahedron Letters, 28, Chemical and Pharmaceutical Bulletin, 36, Tetrahedron, 44, Drugs, 42, Synthetic Communications, 20, Chinese Journal of Organic Chemistry, 22, Synthetic Communications, 30, Iranian Journal of Chemistry and Chemical Engineering, 20, Indian Journal of Chemistry, 46B, Journal of the Chemical Society of Pakistan, 31, The Journal of American Science, 8, Chemical Science Transactions, 2, Heterocycles, 32, Journal of the American Chemical Society, 74, The Journal of Organic Chemistry, 51, The Journal of Organic Chemistry, 26, Synthetic Communications, 39, Chemistry of Heterocyclic Compounds, 35, Journal of the Serbian Chemical Society, 74, Research Journal of Chemical Sciences, 1, The Journal of Organic Chemistry, 11, Journal of Applied Sciences, 2, Chinese Chemical Letters, 20, Chinese Chemical Letters, 21, Croatica Chemica Acta, 84, Indian Journal of Chemistry, 50B, Share This Article:.

The paper is not in the journal. Go Back HomePage. Abstract PP. DOI: Also, it demonstrates the reactivity of these arylidene derivatives in heterocyclic synthesis with emphasis on the most recent findings.

Volume 60: Oxazoles. Synthesis, Reactions, and Spectroscopy, Part A

The others are synthetic substances which are convenient and important intermediates for the synthesis of a variety of useful and novel heterocyclic systems. Conflicts of Interest The authors declare no conflicts of interest. Cite this paper El-Gohary, N. Open Access Library Journal , 1 , References [ 1 ] Choudary, B. Please enable JavaScript to view the comments powered by Disqus. OALibJ Subscription. E-Mail Alert.

Chemistry of Heterocyclic Compounds

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Volume 62: The Chemistry of 1,2,3-Thiadiazoles

Choudary, B. Prajapati, D. Khan, R. Tanaka, K. Obrador, E. Balalaie, S. Loupy, A. Maggi, R. Bigi, F.

Rupe, H. Hermes, S. Breslow, D. Kazauki, K. Obara, H. Gaissman, T. Martin, G. Crawley, L. Patil, C.