Synthesis of 2,5-bis-(4-cyanophenyl)-furan

Heterocyclic Communications

Volumn 2, Issue 2, 1996, Pages 135-140

  Bajic, Marina ^a   Kumar, Arvind ^a   Boykin, David W ^a  

^a GEORGIA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001173212     PISSN: 07930283     EISSN: None     Source Type: Journal    
DOI: 10.1515/HC.1996.2.2.135     Document Type: Article

References (14)

1. B. P. Das and D. W. Boykin, J. Med. Chem. 20, 531 (1977)
2. D. W. Boykin, A. Kumar, J. Spychala, M. Zhou, R. J. Lombardy, W. D. Wilson, C. C. Dykstra, S. K. Jones, J. E. Hall, R. R. Tidwell, C. Laughton, C. M. Nunn and S. Neidle, J. Med. Chem. 38, 912 (1995)
3. W. D. Wilson, F. A. Tanious, H. Buczak, L. S. Ratmeyer, M. K. Venkatramanan, A. Kumar, D. W. Boykin and B. R. Munson, "Molecular Factors that Control the Nucleic Acid Binding Mode Selection of Unfused Aromatic Cations", in Structure and Function, Nucleic Acids, Vol. 1, eds. M. H. Sarma and R. H. Sarma, Adenine Press, 83-105, (1992)
4. F. A. Tanious, J. Spychala, A. Kumar, K. Greene, D. W. Boykin and W. D. Wilson, J. Biomol. Struct Dyn. 11, 1063 (1994)
5. M. Zhao, L. Ratmeyer, R. G. Peloquin, S. Yao, A. Kumar, J. Spychala, D. W. Boykin and W. D. Wilson, Bioorganic and Med. Chem. 3, 785 (1995)
6. Y. Ito, T. Kokonike and T. Saegusa, J. Am. Chem. Soc. 99, 1487 (1977)
7. R. M. Dessau and E. I. Heiba, J. Org. Chem. 39, 3457 (1974)
8. R. Moriarty, O. Prakash and M. P. Duncan, J. Chem. Soc. Perkin Trans. I, 559 (1987)
9. R. E. Lutz and W. M. Eisner, J. Am. Chem. 56, 2698 (1939)
10. H. Stetter and H.-J. Bender, Angew. Chem. Int. Ed. Engl. 17, 131 (1978)
11. H. Stetter and H.-J. Bender, Chem. Ber. 114, 126 (1981)
12. H. Stetter and H. Kuhlmann, "The Catalyzed Nucleophilic Addition of Aldehydes to Elecctrophilic Double Bonds" in Organic Reactions, ed. L. Paquette, Vol. 40, 407 (1991)
13. We also explored the reaction of 4-cyanobenzenediazonium chloride with 5-(4-cyanophenyl)-2-furoic acid under Meerwein conditions and found that 1 was formed in low yields (25 %). cf. E. Meerwein, J. Prakt. Chem. 152, 239 (1939) and A. Krutosikova, J. Kovac and V. Sykora, Coll. Czech. Chem. Commun., 39, 1892 (1974)
14. We also explored the reaction of 4-cyanobenzenediazonium chloride with 5-(4-cyanophenyl)-2-furoic acid under Meerwein conditions and found that 1 was formed in low yields (25 %). cf. E. Meerwein, J. Prakt. Chem. 152, 239 (1939) and A. Krutosikova, J. Kovac and V. Sykora, Coll. Czech. Chem. Commun., 39, 1892 (1974)