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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Michael G. Organ

Department of Chemistry

York University

4700 Keele Street

Toronto

[email]@yorku.ca

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Chemistry, York University, 4700 Keele Street, Toronto. 2000 - 2012

References

  1. Sterically demanding imidazolinium salts through the activation and cyclization of formamides. Tsimerman, M., Mallik, D., Matsuo, T., Otani, T., Tamao, K., Organ, M.G. Chem. Commun. (Camb.) (2012) [Pubmed]
  2. Pd-catalyzed aryl amination mediated by well defined, N-heterocyclic carbene (NHC)-Pd precatalysts, PEPPSI. Organ, M.G., Abdel-Hadi, M., Avola, S., Dubovyk, I., Hadei, N., Kantchev, E.A., O'Brien, C.J., Sayah, M., Valente, C. Chemistry (2008) [Pubmed]
  3. Formation of substituted pyrroles via an imine condensation/Aza-Claisen rearrangement/imine-allene cyclization process by MAOS. Bremner, W.S., Organ, M.G. J. Comb. Chem (2008) [Pubmed]
  4. Biaryls made easy: PEPPSI and the Kumada-Tamao-Corriu reaction. Organ, M.G., Abdel-Hadi, M., Avola, S., Hadei, N., Nasielski, J., O'brien, C.J., Valente, C. Chemistry (2007) [Pubmed]
  5. A user-friendly, all-purpose Pd-NHC (NHC=N-heterocyclic carbene) precatalyst for the negishi reaction: a step towards a universal cross-coupling catalyst. Organ, M.G., Avola, S., Dubovyk, I., Hadei, N., Kantchev, E.A., O'Brien, C.J., Valente, C. Chemistry (2006) [Pubmed]
  6. On the regiochemistry of nucleophilic attack on 2-halo pi-allyl complexes. 4. The effect of silver acetate and nucleophile concentrations in competitive nucleophilic attack with malonate and phenoxide nucleophiles. Organ, M.G., Arvanitis, E.A., Hynes, S.J. J. Org. Chem. (2003) [Pubmed]
  7. The synthesis of deoxyfusapyrone. 2. Preparation of the bis-trisubstituted olefin fragment and its attachment to the pyrone moiety. Organ, M.G., Wang, J. J. Org. Chem. (2003) [Pubmed]
  8. Combining the use of solid-supported transition metal catalysis with microwave irradiation in solution-phase parallel library synthesis. Organ, M.G., Mayer, S., Lepifre, F., N'Zemba, B., Khatri, J. Mol. Divers. (2003) [Pubmed]
  9. The use of a supported base and strong cation exchange (SCX) chromatography to prepare a variety of structurally-diverse molecular libraries prepared by solution-phase methods. Organ, M.G., Dixon, C.E., Mayhew, D., Parks, D.J., Arvanitis, E.A. Comb. Chem. High Throughput Screen. (2002) [Pubmed]
  10. Approach toward the total synthesis of orevactaene. 2. Convergent and stereoselective synthesis of the C18-C31 domain of orevactaene. Evidence for the relative configuration of the side chain. Organ, M.G., Bilokin, Y.V., Bratovanov, S. J. Org. Chem. (2002) [Pubmed]
  11. A concise synthesis of silanediol-based transition-state isostere inhibitors of proteases. Organ, M.G., Buon, C., Decicco, C.P., Combs, A.P. Org. Lett. (2002) [Pubmed]
  12. The synthesis of deoxyfusapyrone. 1. An approach to the pyrone moiety. Organ, M.G., Wang, J. J. Org. Chem. (2002) [Pubmed]
  13. Synthesis of stereodefined polysubstituted olefins. 1. Sequential intermolecular reactions involving selective, stepwise insertion of Pd(0) into allylic and vinylic halide bonds. The stereoselective synthesis of disubstituted olefins. Organ, M.G., Cooper, J.T., Rogers, L.R., Soleymanzadeh, F., Paul, T. J. Org. Chem. (2000) [Pubmed]
 
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