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William von E. Doering

Prof. Doering maintains a modest research activity in physical, mechanistic organic chemistry involving at any one time no more than two postdoctoral associates. Current research focuses on factors that influence the fate of the diradicals that mediate product distribution in not-obviously concerted reactions. The nature of the transition region of very strongly concerted 1,5-dienyl hydrogen shifts is being probed by examining response to radical-stabilizing groups.


Selected Publications

1. Conformational Restraint in Thermal Rearrangements of a Cyclobutane: 3,4-Dicyanotricyclo[4.2.2.02,5]decane
  Doering, W. v. E.; DeLuca, J. P. J. Am. Chem. Soc. 2003, 125, 10608-10614
 
2. Fate of Diradicals in the Caldera: Stereochemistry of Stereomutation and Ring Enlargement in cis- and trans-1-Cyano-2(E)-propenylycyclopropanes
  Doering, W. v. E.; Barsa, E. A., J. Am. Chem. Soc., 2004, 126, 12353-12362
 
3. Perturbations by Phenyl on the 1,5-Hydrogen Shift in 1,3(Z)-Pentadiene. Another Chameleonic Transition Region?
  Doering, W. v. E.; Keliher, E. J.; Zhao, X., J. Am. Chem. Soc., 2004, 126, 14206-14216
 
4. Pressure Independence of Stereomutation and Fragmentation in the Bis-spirocyclobutanes, anti- and syn-2,9-Dicyanodispiro[5.0.5.2]tetradeca-1,8-dienes
  Klärner, F.-G.; Wurche, F.; Doering, W. v. E.; Yang, J.-d., J. Am. Chem. Soc., 2005, 127, 18107-18113
 
5. Kinetics of Thermal Rearrangements in the 2-Thujene System: A Full Quadrisection of a Perturbed Bicyclo[3.1.0]hex-2-ene
  Doering, W. v. E.; Zhang, T.-h.; Schmidt, E. K. G., J. Org. Chem., 2006, 5688-5693
 
6. Effect of Kinetics by Deuterium in the 1,5-Hydrogen Shift of a Cisoid-Locked 1,3(Z)-Pentadiene, 2-Methyl-10-methylenebicyclo[4.4.0]deca-1-ene; Evidence for Tunneling?
  Doering, W. v. E.; Zhao, X., J. Am. Chem. Soc., 2006, 128, 9080-9085
 
Supported by WDS