All Stories

  1. Spiro-Lactams as Novel Antimicrobial Agents
  2. 1,3-Dipolar Cycloadditions Involving Allenes: Synthesis of Five-Membered Rings
  3. Phosphane-Catalyzed [3+2] Annulation of Allenoates with 3-Nitro-2H -chromenes: Synthesis of Tetrahydrocyclopenta[c ]chromenes
  4. Molecular and crystal structures and spectroscopic properties of 2-oxo-2-(Thiophen-2-yl) ethyl phosphonic acid
  5. ONE-POT DIASTEREOSELECTIVE SYNTHESIS OF CHIRAL TRICYCLIC l-CYSTEINE AND d-PENICILLAMINE DERIVATIVES: A LABORATORY EXPERIMENT
  6. Cholesteryl hemiesters alter lysosome structure and function and induce proinflammatory cytokine production in macrophages
  7. Conformational behaviour, photochemistry and flash vacuum pyrolysis of a 2-(1H-tetrazol-1-yl)thiophene
  8. Synthesis of Thieno[2,3-d]pyrimidines via Microwave-Assisted Thermolysis of 1-(Thiophene-2-yl)-1H-tetrazoles
  9. Synthesis and thermal reactivity of thiazolo[3,4-a]benzimidazole-2,2-dioxides: approach to 1H-benzo[d]imidazoles via novel benzo-2,5-diazafulvenium methides
  10. Thermolysis of 1-(thiophen-2-yl)-1H-tetrazoles: a route to thiophene-fused imidazoles and pyrimidines
  11. Pericyclic Reactions of Azafulvenium Methides Bearing Internal Dipolarophiles - Synthesis of Chromene and Chromane Derivatives
  12. 742: Chiral 6,7-bis(hydroxymethyl)-1H,3H-pyrrolo[1,2-c]thiazoles as anticancer agents against breast cancer MCF7 and HCC1806 cell lines
  13. 741: PARP-inhibitor PJ34 potentiates the anticancer effect of chiral 6,7-bis(hydroxymethyl)-1H,3H-pyrrolo[1,2-c]thiazoles against breast cancer cell lines
  14. Targeting triple-negative breast cancer cells with 6,7-bis(hydroxymethyl)-1H,3H-pyrrolo[1,2-c]thiazoles
  15. Microwave-induced Pericyclic Reactions of Aza- and Diazafulvenium Methides
  16. Chiral 6,7-bis(hydroxymethyl)-1H,3H-pyrrolo[1,2-c]thiazoles with anti-breast cancer properties
  17. Thiazolo[3,4-b]indazole-2,2-dioxides as Masked Extended Dipoles: Pericyclic Reactions of Benzodiazafulvenium Methides
  18. Nitrogen-bridged heterocycles via cycloaddition of non-classical heterocyclic-fused-[c]thiazoles
  19. Chiral 6-hydroxymethyl-1H,3H-pyrrolo[1,2-c]thiazoles: Novel antitumor DNA monoalkylating agents
  20. Novel antitumor DNA monoalkylating agents: Synthesis and biological evaluation
  21. Flash vacuum pyrolysis of 2,2-dioxo-1H,3H-pyrrolo[1,2-c]thiazoles and 2-vinyl-1H-pyrroles
  22. Microwave-assisted generation and reactivity of aza- and diazafulvenium methides: heterocycles via pericyclic reactions
  23. Chemistry of Diazafulvenium Methides in the Synthesis of Functionalized Pyrazoles
  24. ‘Higher-order’ azomethine ylides in the synthesis of functionalized pyrroles and 5-oxo-5H-pyrrolizines
  25. Conformational Behavior of Dimethyl 5-Methyl-1H,3H-pyrrolo[1,2-c][1,3]thiazole-6,7-dicarboxylate 2,2-Dioxide Isolated in Low-Temperature Matrixes
  26. New chemistry of diazafulvenium methides: one way to pyrazoles
  27. N-Vinyl- and C-Vinylpyrroles from Azafulvenium Methides. Flash Vacuum Pyrolysis Route to 5-Oxo-5H-pyrrolizines and 1-Azabenzo[f]azulenes
  28. Reactivity of azafulvenium methides derived from pyrrolo[1,2-c]thiazole-2,2-dioxides: synthesis of functionalised pyrroles
  29. Synthesis of Chiral Pyrrolo[1,2-c]thiazoles via Intramolecular Dipolar Cycloaddition of Münchnones:  An Interesting Rearrangement to Pyrrolo[1,2-c]thiazines