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Jeffrey T. Kuethe

Department of Process Research

Merck & Co. Inc.

Rahway

NJ 07065

USA

[email]@merck.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Process Research, Merck & Co. Inc., Rahway, NJ 07065, USA. 2003 - 2007

References

  1. A concise synthesis of (S)-N-ethoxycarbonyl-alpha-methylvaline. Kuethe, J.T., Gauthier, D.R., Beutner, G.L., Yasuda, N. J. Org. Chem. (2007) [Pubmed]
  2. Asymmetric Diels-Alder reactions of chiral cyclopropylidene imide dienophiles: preparation of gem-dimethyl- and spirocyclopropane norbornyl carboxylic acids. Kuethe, J.T., Zhao, D., Humphrey, G.R., Journet, M., McKeown, A.E. J. Org. Chem. (2006) [Pubmed]
  3. Stereoselective preparation of a cyclopentane-based NK1 receptor antagonist bearing an unsymmetrically substituted sec-sec ether. Kuethe, J.T., Marcoux, J.F., Wong, A., Wu, J., Hillier, M.C., Dormer, P.G., Davies, I.W., Hughes, D.L. J. Org. Chem. (2006) [Pubmed]
  4. Synthesis of 5-substituted-1H-indol-2-yl-1H-quinolin-2-ones: a novel class of KDR kinase inhibitors. Kuethe, J.T., Wong, A., Qu, C., Smitrovich, J., Davies, I.W., Hughes, D.L. J. Org. Chem. (2005) [Pubmed]
  5. A rapid synthesis of 2-aryl-5-substituted-2,3-dihydrobenzofurans. Kuethe, J.T., Wong, A., Journet, M., Davies, I.W. J. Org. Chem. (2005) [Pubmed]
  6. Synthesis of disubstituted imidazo[4,5-b]pyridin-2-ones. Kuethe, J.T., Wong, A., Davies, I.W. J. Org. Chem. (2004) [Pubmed]
  7. Effective strategy for the preparation of indolocarbazole aglycons and glycosides: total synthesis of tjipanazoles B, D, E, and I. Kuethe, J.T., Wong, A., Davies, I.W. Org. Lett. (2003) [Pubmed]
 
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