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Tiazole (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "Tiazole" in Catalan language version.

refsWebsite
Global rank Catalan rank
3doi.org
2nd place
6th place
3nih.gov
4th place
7th place
2orgsyn.org
2,971st place
2,672nd place

doi.org

dx.doi.org

  • Alajarín, M.; Cabrera, J.; Pastor, A.; Sánchez-Andrada, P.; Bautista, D. «On the [2+2] Cycloaddition of 2-Aminothiazoles and Dimethyl Acetylenedicarboxylate. Experimental and Computational Evidence of a Thermal Disrotatory Ring Opening of Fused Cyclobutenes». J. Org. Chem., 71, 14, 2006, pàg. 5328–5339. DOI: 10.1021/jo060664c. PMID: 16808523.
  • Elizabeta Amir and Shlomo Rozen «Easy access to the family of thiazole N-oxides using HOF·CH3CN». Chemical Communications, 2006, 21, 2006, pàg. 2262–2264. DOI: 10.1039/b602594c. PMID: 16718323.
  • Mateo Alajarín, José Cabrera, Aurelia Pastor, Pilar Sánchez-Andrada, and Delia Bautista «On the [2+2] Cycloaddition of 2-Aminothiazoles and Dimethyl Acetylenedicarboxylate. Experimental and Computational Evidence of a Thermal Disrotatory Ring Opening of Fused Cyclobutenes». J. Org. Chem., 71, 14, 2006, pàg. 5328–5339. DOI: 10.1021/jo060664c. PMID: 16808523.

nih.gov

ncbi.nlm.nih.gov

  • Alajarín, M.; Cabrera, J.; Pastor, A.; Sánchez-Andrada, P.; Bautista, D. «On the [2+2] Cycloaddition of 2-Aminothiazoles and Dimethyl Acetylenedicarboxylate. Experimental and Computational Evidence of a Thermal Disrotatory Ring Opening of Fused Cyclobutenes». J. Org. Chem., 71, 14, 2006, pàg. 5328–5339. DOI: 10.1021/jo060664c. PMID: 16808523.
  • Elizabeta Amir and Shlomo Rozen «Easy access to the family of thiazole N-oxides using HOF·CH3CN». Chemical Communications, 2006, 21, 2006, pàg. 2262–2264. DOI: 10.1039/b602594c. PMID: 16718323.
  • Mateo Alajarín, José Cabrera, Aurelia Pastor, Pilar Sánchez-Andrada, and Delia Bautista «On the [2+2] Cycloaddition of 2-Aminothiazoles and Dimethyl Acetylenedicarboxylate. Experimental and Computational Evidence of a Thermal Disrotatory Ring Opening of Fused Cyclobutenes». J. Org. Chem., 71, 14, 2006, pàg. 5328–5339. DOI: 10.1021/jo060664c. PMID: 16808523.

orgsyn.org