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Luis R. Domingo

Departamento de Química Orgánica

Universidad de Valencia

Dr. Moliner 50

E-46100 Burjassot

Spain

[email]@utopia.uv.es

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Departamento de Química Orgánica, Universidad de Valencia, Dr. Moliner 50, E-46100 Burjassot, Spain. 2001 - 2012
  • Instituto de Ciencia Molecular/Departamento de Química Orgánica, Universidad de Valencia, Polígono La Coma s/n, 46980 Paterna, Spain. 2006

References

  1. Understanding the mechanism of the intramolecular stetter reaction. A DFT study. Domingo, L.R., Zaragozá, R.J., Saéz, J.A., Arnó, M. Molecules (2012) [Pubmed]
  2. Understanding the cooperative NHC/LA catalysis for stereoselective annulation reactions with homoenolates. A DFT study. Domingo, L.R., Zaragozá, R.J., Arnó, M. Org. Biomol. Chem. (2011) [Pubmed]
  3. DFT study on the cycloreversion of thietane radical cations. Domingo, L.R., Pérez-Ruiz, R., Argüello, J.E., Miranda, M.A. J. Phys. Chem. A (2011) [Pubmed]
  4. Understanding the mechanism of stereoselective synthesis of cyclopentenes via N-heterocyclic carbene catalyzed reactions of enals with enones. Domingo, L.R., Zaragozá, R.J., Arnó, M. Org. Biomol. Chem. (2010) [Pubmed]
  5. DFT study of the molecular mechanism of Lewis acid induced [4 + 3] cycloadditions of 2-alkylacroleins with cyclopentadiene. Domingo, L.R., Arnó, M., Sáez, J.A. J. Org. Chem. (2009) [Pubmed]
  6. Understanding the mechanism of polar Diels-Alder reactions. Domingo, L.R., Sáez, J.A. Org. Biomol. Chem. (2009) [Pubmed]
  7. DFT study on the molecular mechanism of the [4 + 2] cycloaddition between thiobenzophenone and arylalkenes via radical cations. Domingo, L.R., Pérez-Ruiz, R., Argüello, J.E., Miranda, M.A. J. Phys. Chem. A (2009) [Pubmed]
  8. Toward an understanding of the unexpected regioselective hetero-Diels-Alder reactions of asymmetric tetrazines with electron-rich ethylenes: a DFT study. Domingo, L.R., Picher, M.T., Sáez, J.A. J. Org. Chem. (2009) [Pubmed]
  9. Understanding the participation of quadricyclane as nucleophile in polar [2sigma + 2sigma + 2pi] cycloadditions toward electrophilic pi molecules. Domingo, L.R., Saéz, J.A., Zaragozá, R.J., Arnó, M. J. Org. Chem. (2008) [Pubmed]
  10. Understanding the reactivity of captodative ethylenes in polar cycloaddition reactions. A theoretical study. Domingo, L.R., Chamorro, E., Pérez, P. J. Org. Chem. (2008) [Pubmed]
  11. Toward an understanding of the acceleration of Diels-Alder reactions by a pseudo-intramolecular process achieved by molecular recognition. A DFT study. Domingo, L.R., Aurell, M.J., Arnó, M., Saez, J.A. J. Org. Chem. (2007) [Pubmed]
  12. 1,3-Dipolar cycloadditions of electrophilically activated benzonitrile N-oxides. Polar cycloaddition versus oxime formation. Domingo, L.R., Picher, M.T., Arroyo, P., Saez, J.A. J. Org. Chem. (2006) [Pubmed]
  13. Exploring two-state reaction pathways in the photodimerization of cyclohexadiene. Domingo, L.R., Pérez-Prieto, J. Chemphyschem (2006) [Pubmed]
  14. Studies on the biosynthesis of paraherquamide A and VM99955. A theoretical study of intramolecular Diels-Alder cycloaddition. Domingo, L.R., Zaragozá, R.J., Williams, R.M. J. Org. Chem. (2003) [Pubmed]
  15. Origin of the synchronicity on the transition structures of polar Diels-Alder reactions. Are these reactions [4 + 2] processes?. Domingo, L.R., José Aurell, M., Pérez, P., Contreras, R. J. Org. Chem. (2003) [Pubmed]
  16. Electronic contributions to the sigma(p) parameter of the Hammett equation. Domingo, L.R., Pérez, P., Contreras, R. J. Org. Chem. (2003) [Pubmed]
  17. Enhancing reactivity of carbonyl compounds via hydrogen-bond formation. A DFT study of the hetero-Diels-Alder reaction between butadiene derivative and acetone in chloroform. Domingo, L.R., Andrés, J. J. Org. Chem. (2003) [Pubmed]
  18. Density functional theory study of the cycloaddition reaction of furan derivatives with masked o-benzoquinones. Does the furan act as a dienophile in the cycloaddition reaction?. Domingo, L.R., Aurell, M.J. J. Org. Chem. (2002) [Pubmed]
  19. A theoretical study of the molecular mechanism of the reaction between N,N-dimethylmethyleneammonium cation and cyclopentadiene. Domingo, L.R. J. Org. Chem. (2001) [Pubmed]
  20. A theoretical study of the reaction between cyclopentadiene and protonated imine derivatives: a shift from a concerted to a stepwise molecular mechanism. Domingo, L.R., Oliva, M., Andrés, J. J. Org. Chem. (2001) [Pubmed]
 
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