Synthesis of biologically active heterocycles from coumarin thiocyanate

Acta Poloniae Pharmaceutica - Drug Research

Volumn 68, Issue 3, 2011, Pages 441-446

  Langi, Bhushan P ^a   Mulwad, Vinata V ^a   Chaskar, Atul C ^a  

^a INSTITUTE OF SCIENCE   (India)

Author keywords

Antimicrobial activity; Oxathiazine; Oxathiole; Thiadiazin; Thiocyanate

Indexed keywords

2 IMINO 8 METHYL 4H 1,3 OXATHIOL[4,5 C]BENZOPYRAN 4 ONE; 2,4 DIAMINO 10 METHYL 6H BENZOPYRAN[4,3 F] 1,3,5 THIADIAZEPIN 6 ONE; 3 AMINO 9 METHYL 5H BENZOPYRAN[3,4 E] 1,2,4 OXATHIAZIN 5 ONE; 3 AMINO 9 METHYL 5H BENZOPYRAN[4,3 E] 1,3,4 THIADIAZIN 5 ONE; 4 HYDROXY 6 METHYL 2 OXO 2H BENZOPYRAN 3 YL THIOCYANATE; 8 METHYL 4H,2H 1,3 OXATHIOL[4,5 C]BENZOPYRAN 2,4 DIONE; COUMARIN DERIVATIVE; COUMARIN THIOCYANATE; HETEROCYCLIC COMPOUND; OXATHIAZINE; OXATHIOL; STREPTOMYCIN; THIADIAZEPINE; THIADIAZINE DERIVATIVE; THIAZINE DERIVATIVE; THIOCYANIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CHEMICAL REACTION; CONTROLLED STUDY; CYANATION; DRUG DIFFUSION; DRUG SYNTHESIS; ESCHERICHIA COLI; NONHUMAN; SALMONELLA TYPHIMURIUM; STAPHYLOCOCCUS AUREUS;

ANTI-INFECTIVE AGENTS; COUMARINS; DISK DIFFUSION ANTIMICROBIAL TESTS; ESCHERICHIA COLI; MOLECULAR STRUCTURE; SALMONELLA TYPHI; STAPHYLOCOCCUS AUREUS; STRUCTURE-ACTIVITY RELATIONSHIP; THIOCYANATES;

EID: 79956323486     PISSN: 00016837     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)

1. (a) Wood J.L.: Org. React. 3, 240, (1946);
2. (b) Kelly T.R., Kim M.H., Curtis A.D.M.: J. Org. Chem. 58, 5855 (1993).
3. Mehta R.G., Liu J., Constantinou A., Thomas C.F., Hawthorne M., You M., Gerhaeusers C., et al.: Carcinogenesis 16, 399, (1995).
4. (a) Leblanc B.L., Jursic B.C.: Synth. Commun. 28, 3591 (1998);
5. st edn., Academic Press, London 1975.
6. Chande M.S., Dravid R.N.: Indian Acad. Sci. (Chem. Sci.), 100, 53 (1988).
7. Muelus S., Rossanna D.M., Hugo C., Gustavo S., Carmen O.: Folia Parasitol. 48, 105 (2001).
8. Atienza J., Martínez Díaz R.A., Gómez Barrio A., Escario J.A., Herrero A., Ochoa C., Rodríguez J.: Chemotherapy 38, 441 (1992).
9. Katiyar D., Tiwari V.K., Tripathi R.P., Srivastava A., Chaturvedi V., Srivastava R., Srivastava B.S.: Bioorg. Med. Chem. 11, 4369 (2003).
10. Esteban A. I., Clercq E. De., Martinez A.: Nucleosides Nucleotides Nucleic Acids 16, 265 (1997).
11. Konieczny M.T., Konieczny W., Sabisz M., Składanowski A., Wakieć R. et al.: Eur. J. Med. Chem. 42, 729 (2007).
12. Yadav S., Tripathi R.K., Dwivedi R., Singh H.: J. Agric. Food Chem. 40, 1700 (1992).
13. Peter R.H., Chao Wan-Ru, Sato B., Shigeno K., Zaveri N.T., Tanabe M.: Steroids 68, 97 (2003).
14. (a) Borsini F.: EP Pat, 0, 354, 885, (1990);
15. (b) Weber A., Frossard J.: Ann. Pharm. Franc. 24, 445 (1966).
16. Kumar A., Ahmad P., Maurya R. A.: Tetrahedron Lett. 48, 1399 (2007)