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Francisco Sarabia

Department of Organic Chemistry

Faculty of Sciences

University of Malaga

Campus de Teatinos s/n. 29071 Malaga (Spain)

[email]@uma.es

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Organic Chemistry, Faculty of Sciences, University of Malaga, Campus de Teatinos s/n. 29071 Malaga (Spain). 2003 - 2012

References

  1. A highly stereoselective synthesis of glycidic amides based on a new class of chiral sulfonium salts: applications in asymmetric synthesis. Sarabia, F., Vivar-García, C., García-Castro, M., García-Ruiz, C., Martín-Gálvez, F., Sánchez-Ruiz, A., Chammaa, S. Chemistry (2012) [Pubmed]
  2. Cyclic sulfur ylides derived from Gleason-type chiral auxiliaries for the asymmetric synthesis of epoxy amides. Sarabia, F., Vivar-García, C., García-Castro, M., Martín-Ortiz, J. J. Org. Chem. (2011) [Pubmed]
  3. Solid phase synthesis of globomycin and SF-1902 A5. Sarabia, F., Chammaa, S., García-Ruiz, C. J. Org. Chem. (2011) [Pubmed]
  4. Chiral sulfur ylides for the synthesis of bengamide E and analogues. Sarabia, F., Martín-Gálvez, F., Chammaa, S., Martín-Ortiz, L., Sánchez-Ruiz, A. J. Org. Chem. (2010) [Pubmed]
  5. A highly efficient methodology of asymmetric epoxidation based on a novel chiral sulfur ylide. Sarabia, F., Chammaa, S., García-Castro, M., Martín-Gálvez, F. Chem. Commun. (Camb.) (2009) [Pubmed]
  6. Epoxyamide-based strategy for the synthesis of polypropionate-type frameworks. Sarabia, F., Martín-Gálvez, F., García-Castro, M., Chammaa, S., Sánchez-Ruiz, A., Tejón-Blanco, J.F. J. Org. Chem. (2008) [Pubmed]
  7. Stereoselective synthesis of macrolide-type antibiotics from epoxy amides. Synthesis of the polypropionate chain of streptovaricin u. Sarabia, F., Sánchez-Ruiz, A., Martín-Ortiz, L., García-Castro, M., Chammaa, S. Org. Lett. (2007) [Pubmed]
  8. Stereoselective synthesis of E-64 and related cysteine proteases inhibitors from 2,3-epoxyamides. Sarabia, F., Sánchez-Ruiz, A., Chammaa, S. Bioorg. Med. Chem. (2005) [Pubmed]
  9. Total synthesis of Bengamide E and analogues by modification at C-2 and at terminal olefinic positions. Sarabia, F., Sánchez-Ruiz, A. J. Org. Chem. (2005) [Pubmed]
  10. Synthetic studies on stevastelins. 1. Total synthesis of stevastelins B and B3. Sarabia, F., Chammaa, S. J. Org. Chem. (2005) [Pubmed]
  11. Synthetic studies on stevastelins. 2. Synthesis of lipidic- and peptidic-modified analogues. Sarabia, F., Chammaa, S., García-Castro, M. J. Org. Chem. (2005) [Pubmed]
  12. Chemistry and biology of cyclic depsipeptides of medicinal and biological interest. Sarabia, F., Chammaa, S., Ruiz, A.S., Ortiz, L.M., Herrera, F.J. Curr. Med. Chem. (2004) [Pubmed]
  13. A convergent synthetic approach to the nucleoside-type liposidomycin antibiotics. Sarabia, F., Martín-Ortiz, L., López-Herrera, F.J. Org. Lett. (2003) [Pubmed]
 
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