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Collect. Czech. Chem. Commun. 1991, 56, 2340-2351
https://doi.org/10.1135/cccc19912340

Synthesis of the six isomeric thieno[c]-fused 1,5- and 1,6-naphthyridines

Salo Gronowitz*, Johan Malm and Anna-Britta Hörnfeldt

Organic Chemistry 1, Chemical Center, Lund University, Box 124, S-221 00 Lund, Sweden

Crossref Cited-by Linking

  • Saha Pritam: Microwave Irradiated, Sodium Aluminate Supported and Zinc Catalyzed Suzuki-Miyaura Cross-Coupling Reaction on Fused Tricyclic Oxa-Aza-Quinolone: A Green Protocol. AMM 2023, 911, 3. <https://doi.org/10.4028/p-lanj11>
  • Sahu Krishnendu B., Maity Arindam, Mondal Shyamal, Paira Rupankar, Saha Pritam, Naskar Subhendu, Hazra Abhijit, Banerjee Sukdeb, Mondal Nirup B.: Basic Alumina‐Supported Synthesis of Aryl‐Heteroarylmethanes via Palladium Catalyzed Cross‐Coupling under Microwave Irradiation. Journal of Heterocyclic Chem 2013, 50. <https://doi.org/10.1002/jhet.1099>
  • Saha Pritam, Naskar Subhendu, Paira Priyankar, Hazra Abhijit, Sahu Krishnendu B., Paira Rupankar, Banerjee Sukdeb, Mondal Nirup B.: Basic alumina-supported highly effective Suzuki–Miyaura cross-coupling reaction under microwave irradiation: application to fused tricyclic oxa-aza-quinolones. Green Chem. 2009, 11, 931. <https://doi.org/10.1039/b902916h>
  • Fleckenstein Christoph A., Plenio Herbert: Efficient Suzuki−Miyaura Coupling of (Hetero)aryl Chlorides with Thiophene- and Furanboronic Acids in Aqueous n-Butanol. J. Org. Chem. 2008, 73, 3236. <https://doi.org/10.1021/jo8001886>
  • Litvinov Victor P, Roman Sergey V, Dyachenko Vladimir D: Naphthyridines. Structure, physicochemical properties and general methods of synthesis. Russ. Chem. Rev. 2000, 69, 201. <https://doi.org/10.1070/RC2000v069n03ABEH000553>
  • Aakermann Torunn, Gronowitz Salo: SYNTHESIS OF TRICYCLIC SYSTEMS OF BIOLOGICAL INTEREST. Heterocyclic Communications 1997, 3. <https://doi.org/10.1515/HC.1997.3.1.7>
  • Björk P, Hörnfeldt A.B., Gronowitz S, Edvardsson U: 4-Substituted 1-(2-methylphenyl)thieno[2,3-c]-1,5-naphthyridines as possible reversible inhibitors of gastric H+,K+-ATPase. European Journal of Medicinal Chemistry 1996, 31, 411. <https://doi.org/10.1016/0223-5234(96)89168-9>
  • Björk Patrick, Aakermann Torunn, Hörnfeldt Anna‐Britta, Gronowitz Salo: Improved syntheses of thieno[2,3‐b]‐ and [3,2‐b]‐fused naphthyridines. Journal of Heterocyclic Chem 1995, 32, 751. <https://doi.org/10.1002/jhet.5570320310>
  • Gronowitz Salo: The versatile chemistry of thiophene. Some contributions by the Gronowitz' group. Chem Heterocycl Compd 1995, 30, 1252. <https://doi.org/10.1007/BF01172861>
  • Malm Johan, Rehn Bengt, Hörnfeldt Anna‐Britta, Gronowitz Salo: Synthesis and nmr spectra of the six isomeric thieno[c]‐fused 1,7‐ and 1,8‐naphthyridines. Journal of Heterocyclic Chem 1994, 31, 11. <https://doi.org/10.1002/jhet.5570310102>
  • Malm Johan, Hörnfeldt Anna‐Britta, Gronowitz Salo: On the bromination of thieno[c]‐fused 1,5‐naphthyridines and their isomeric N‐oxides using dibromoisocyanuric acid in fuming sulfuric acid. Journal of Heterocyclic Chem 1994, 31, 521. <https://doi.org/10.1002/jhet.5570310244>
  • Gronowitz Salo: The versatile chemistry of thiophenes: The effects of b‐side contra c‐side annelation on reactivity. Journal of Heterocyclic Chem 1994, 31, 641. <https://doi.org/10.1002/jhet.5570310306>
  • Björk Patrick, Hörnfeldt Anna‐Britta, Gronowitz Salo: The syntheses and NMR spectra of the twelve isomeric thieno[b]fused naphthyridines. Journal of Heterocyclic Chem 1994, 31, 1161. <https://doi.org/10.1002/jhet.5570310511>
  • Gronowitz Salo, Björk Patrick, Malm Johan, Hörnfeldt Anna-Britta: The effect of some additives on the Stille Pd0-catalyzed cross-coupling reaction. Journal of Organometallic Chemistry 1993, 460, 127. <https://doi.org/10.1016/0022-328X(93)80368-L>
  • GRONOWITZ S., MALM J., HOERNFELDT A.‐B.: ChemInform Abstract: Synthesis of the Six Isomeric Thieno(c)‐Fused 1,5‐ and 1,6‐ Naphthyridines. ChemInform 1992, 23. <https://doi.org/10.1002/chin.199209214>