Utility of 2-(4,5-dihydro-4-oxothiazol-2-yl)acetonitrile in the synthesis of fused heterocyclic derivatives with anti-tumor activities

Articles in the same Issue

1. Research Articles
2. Biotransformation of a biosynthetic intermediate mimic of nonactin by Streptomyces griseus
3. Selective deprotection of tethered glycoderivatives with unsaturated spacer
4. Synthesis and transformations of novel formyl-substituted quinolines
5. Synthesis and antimalarial activity of Baylis-Hillman adducts from substituted 2-chloroquinoline-3-carboxaldehydes
6. Solvent-free one pot synthesis of indenoquinolinones catalyzed by iron(III) triflate
7. Base-catalyzed three-component synthesis of 2-amino-4,5-dihydro-4-arylpyrano[3,2-b]indole-3-carbonitriles
8. Recyclization reactions of 1-alkylpyrimidinium salts
9. Synthesis of new sulfur-linked di- and triheterocyclic compounds containing thienotriazolopyrimidine and triazolothiadiazole moieties
10. A convenient synthesis of 3- and 5-amino-1H-pyrazoles via 3(5)-amino-4-(ethylsulfinyl)-1H-pyrazole desulfinylation
11. Efficient synthesis of 2,4-disubstituted thiazoles and 2-substituted 4-thiazolidinones under solvent free conditions
12. Regioselective synthesis of 2-[(E)-(benzo[d]thiazol-2(3H)-ylidene)(cyano)methyl]thiazoles
13. Utility of 2-(4,5-dihydro-4-oxothiazol-2-yl)acetonitrile in the synthesis of fused heterocyclic derivatives with anti-tumor activities
14. Spiro indane-1,3-dione pyrrolizidine compounds synthesized by 1,3-dipolar cyclo-addition reaction