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

Huw M. L. Davies

Department of Chemistry

State University of New York at Buffalo 14260

USA

[email]@*.buffalo.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Chemistry, State University of New York at Buffalo 14260, USA. 2000 - 2007
  • Contribution from the Department of Chemistry, University at Buffalo, State University of New York, Buffalo, USA. 2003

References

  1. Balance between allylic C-H activation and cyclopropanation in the reactions of donor/acceptor-substituted rhodium carbenoids with trans-alkenes. Davies, H.M., Coleman, M.G., Ventura, D.L. Org. Lett. (2007) [Pubmed]
  2. Combined C-H activation/cope rearrangement as a strategic reaction in organic synthesis: total synthesis of (-)-colombiasin a and (-)-elisapterosin B. Davies, H.M., Dai, X., Long, M.S. J. Am. Chem. Soc. (2006) [Pubmed]
  3. Direct synthesis of (+)-erogorgiaene through a kinetic enantiodifferentiating step. Davies, H.M., Walji, A.M. Angew. Chem. Int. Ed. Engl. (2005) [Pubmed]
  4. Recent advances in catalytic intramolecular C-H aminations. Davies, H.M., Long, M.S. Angew. Chem. Int. Ed. Engl. (2005) [Pubmed]
  5. Enantioselective double C-H activation of dihydronaphthalenes. Davies, H.M., Jin, Q. Org. Lett. (2005) [Pubmed]
  6. Universal strategy for the immobilization of chiral dirhodium catalysts. Davies, H.M., Walji, A.M. Org. Lett. (2005) [Pubmed]
  7. Lewis acid-catalyzed tandem Diels-Alder reaction/retro-Claisen rearrangement as an equivalent of the inverse electron demand hetero Diels-Alder reaction. Davies, H.M., Dai, X. J. Org. Chem. (2005) [Pubmed]
  8. Catalytic and enantioselective allylic C-H activation with donor-acceptor-substituted carbenoids. Davies, H.M., Nikolai, J. Org. Biomol. Chem. (2005) [Pubmed]
  9. Asymmetric intermolecular C-H functionalization of benzyl silyl ethers mediated by chiral auxiliary-based aryldiazoacetates and chiral dirhodium catalysts. Davies, H.M., Hedley, S.J., Bohall, B.R. J. Org. Chem. (2005) [Pubmed]
  10. Lewis acid induced tandem Diels-Alder reaction/ring expansion as an equivalent of a [4 + 3] cycloaddition. Davies, H.M., Dai, X. J. Am. Chem. Soc. (2004) [Pubmed]
  11. Catalytic asymmetric reactions for organic synthesis: the combined C-H activation/Cope rearrangement. Davies, H.M., Jin, Q. Proc. Natl. Acad. Sci. U.S.A. (2004) [Pubmed]
  12. Synthesis of methylphenidate analogues and their binding affinities at dopamine and serotonin transport sites. Davies, H.M., Hopper, D.W., Hansen, T., Liu, Q., Childers, S.R. Bioorg. Med. Chem. Lett. (2004) [Pubmed]
  13. Simple strategy for the immobilization of dirhodium tetraprolinate catalysts using a pyridine-linked solid support. Davies, H.M., Walji, A.M., Nagashima, T. J. Am. Chem. Soc. (2004) [Pubmed]
  14. Dirhodium(II) tetra(N-(dodecylbenzenesulfonyl)prolinate) catalyzed enantioselective cyclopropenation of alkynes. Davies, H.M., Lee, G.H. Org. Lett. (2004) [Pubmed]
  15. Double C-H activation strategy for the asymmetric synthesis of C2-symmetric anilines. Davies, H.M., Jin, Q. Org. Lett. (2004) [Pubmed]
  16. Enantioselective synthesis of cyclopropylphosphonates containing quaternary stereocenters using a D2-symmetric chiral catalyst Rh2(S-biTISP)2. Davies, H.M., Lee, G.H. Org. Lett. (2004) [Pubmed]
  17. Catalytic asymmetric reactions for organic synthesis: the combined C-H activation/siloxy-cope rearrangement. Davies, H.M., Beckwith, R.E. J. Org. Chem. (2004) [Pubmed]
  18. Asymmetric intermolecular C-H activation, using immobilized dirhodium tetrakis((S)-N-(dodecylbenzenesulfonyl)- prolinate) as a recoverable catalyst. Davies, H.M., Walji, A.M. Org. Lett. (2003) [Pubmed]
  19. Dirhodium tetraprolinate-catalyzed asymmetric cyclopropanations with high turnover numbers. Davies, H.M., Venkataramani, C. Org. Lett. (2003) [Pubmed]
  20. New strategic reactions for organic synthesis: catalytic asymmetric C-H activation alpha to nitrogen as a surrogate for the mannich reaction. Davies, H.M., Venkataramani, C., Hansen, T., Hopper, D.W. J. Am. Chem. Soc. (2003) [Pubmed]
  21. Catalytic asymmetric benzylic C-H activation by means of carbenoid-induced C-H insertions. Davies, H.M., Jin, Q., Ren, P., Kovalevsky, A.Y. J. Org. Chem. (2002) [Pubmed]
  22. Synthesis and monoamine transporter affinity of 3beta-(4-(2-pyrrolyl)phenyl)-8-azabicycl. Davies, H.M., Ren, P., Kong, N., Sexton, T., Childers, S.R. Bioorg. Med. Chem. Lett. (2001) [Pubmed]
  23. Synthesis of 2beta-acyl-3beta-(substituted naphthyl)-8-azabicyclo[3.2.1]octanes and their binding affinities at dopamine and serotonin transport sites. Davies, H.M., Gilliatt, V., Kuhn, L.A., Saikali, E., Ren, P., Hammond, P.S., Sexton, T., Childers, S.R. J. Med. Chem. (2001) [Pubmed]
  24. Asymmetric intramolecular C_H insertions of aryldiazoacetates. Davies, H.M., Grazini, M.V., Aouad, E. Org. Lett. (2001) [Pubmed]
  25. Kinetic resolution and double stereodifferentiation in catalytic asymmetric C-H activation of 2-substituted pyrrolidines. Davies, H.M., Venkataramani, C. Org. Lett. (2001) [Pubmed]
  26. Catalytic asymmetric cyclopropanation of heteroaryldiazoacetates. Davies, H.M., Townsend, R.J. J. Org. Chem. (2001) [Pubmed]
  27. Catalytic asymmetric allylic C-H activation as a surrogate of the asymmetric Claisen rearrangement. Davies, H.M., Ren, P., Jin, Q. Org. Lett. (2001) [Pubmed]
  28. Diastereoselective kinetic protonation of exocyclic enolates derived from bicyclic ketones: control of stereochemistry mediated by bridging heteroatoms. Davies, H.M., Hodges, L.M., Gregg, T.M. J. Org. Chem. (2001) [Pubmed]
  29. Stereoselectivity of methyl aryldiazoacetate cyclopropanations of 1,1-diarylethylene. Asymmetric synthesis of a cyclopropyl analogue of tamoxifen. Davies, H.M., Nagashima, T., Klino, J.L. Org. Lett. (2000) [Pubmed]
 
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