John J. Eisch, Ph.D.
Affiliations: | 2013 | Chemistry | State University of New York, Binghamton, Vestal, NY, United States |
1959-1963 | Chemistry | University of Michigan, Ann Arbor, Ann Arbor, MI |
Area:
organometallic and heterocyclic chemistryWebsite:
http://chemiris.chem.binghamton.edu/EISCH/eisch.htmGoogle:
"John J. Eisch"Bio:
http://um2017.org/faculty-history/faculty/john-j-eisch
http://lib.dr.iastate.edu/rtd/12752
Mean distance: 8.52
Cross-listing: MichiganTree
Parents
Sign in to add mentorHenry Gilman | grad student | 1956 | Iowa State | |
(Comparison of Phenanthridine with Other Aza-aromatic Heterocycles) | ||||
Karl Waldemar Ziegler | post-doc | 1956-1957 | Max-Planck-Institut für Kohlenforschung |
Children
Sign in to add traineeWilliam C. Kaska | grad student | 1963 | University of Michigan |
Fredrick A. Owuor | grad student | 2001 | SUNY Binghamton |
Peter O. Otieno | grad student | 2003 | SUNY Binghamton |
Adetenu A. Adeosun | grad student | 2004 | SUNY Binghamton |
John N. Gitua | grad student | 2005 | SUNY Binghamton |
Paul O. Fregene | grad student | 2007 | SUNY Binghamton |
Kun Yu | grad student | 2013 | SUNY Binghamton |
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Publications
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Eisch JJ, Yu K, Rheingold AL. (2014) Steric factors in the single-electron transfer carbolithiation and transannular reduction of 6,12-diphenyldibenzo[b,f][1,5]diazocine by organolithium reagents European Journal of Organic Chemistry. 2014: 818-832 |
Eisch JJ, Yu K, Rheingold AL. (2012) 6,12-Diphenyldibenzo[b,f][1,5]diazocine as an electron-capture agent: Efficient mechanistic probe for SET processes and reagent for the oxidative dimerization of benzylic organometallics European Journal of Organic Chemistry. 3165-3171 |
Eisch JJ, Gitua JN, Yu K. (2011) Versatile zirconium reductants and carbon-carbon coupling agents selectively accessible from the 2:1 molar aggregate of n-butyllithium and zirconium(IV) salts European Journal of Organic Chemistry. 3523-3530 |
EISCH JJ, MCNULTY JF, SHI X. (2010) ChemInform Abstract: Functionalized Organolithium Reagents. Part 10. Synthesis of Amines via Carbon-Sulfur Bond Cleavages of Substituted Aminomethyl Sulfides with Organolithium Reagents: Aminocarbene Route to Enamines and Sterically Hindered Amines. Cheminform. 25: no-no |
EISCH JJ, MCNULTY JF, SHI X. (2010) ChemInform Abstract: Functionalized Organolithium Reagents. Part 10. Synthesis of Amines via Carbon-Sulfur Bond Cleavages of Substituted Aminomethyl Sulfides with Organolithium Reagents: Aminocarbene Route to Enamines and Sterically Hindered Amines. Cheminform. 25: no-no |
EISCH JJ, MCNULTY JF, SHI X. (2010) ChemInform Abstract: Functionalized Organolithium Reagents. Part 10. Synthesis of Amines via Carbon-Sulfur Bond Cleavages of Substituted Aminomethyl Sulfides with Organolithium Reagents: Aminocarbene Route to Enamines and Sterically Hindered Amines. Cheminform. 25: no-no |
EISCH JJ, MCNULTY JF, SHI X. (2010) ChemInform Abstract: Functionalized Organolithium Reagents. Part 10. Synthesis of Amines via Carbon-Sulfur Bond Cleavages of Substituted Aminomethyl Sulfides with Organolithium Reagents: Aminocarbene Route to Enamines and Sterically Hindered Amines. Cheminform. 25: no-no |
EISCH JJ, MCNULTY JF, SHI X. (2010) ChemInform Abstract: Functionalized Organolithium Reagents. Part 10. Synthesis of Amines via Carbon-Sulfur Bond Cleavages of Substituted Aminomethyl Sulfides with Organolithium Reagents: Aminocarbene Route to Enamines and Sterically Hindered Amines. Cheminform. 25: no-no |
EISCH JJ, MCNULTY JF, SHI X. (2010) ChemInform Abstract: Functionalized Organolithium Reagents. Part 10. Synthesis of Amines via Carbon-Sulfur Bond Cleavages of Substituted Aminomethyl Sulfides with Organolithium Reagents: Aminocarbene Route to Enamines and Sterically Hindered Amines. Cheminform. 25: no-no |
EISCH JJ, MCNULTY JF, SHI X. (2010) ChemInform Abstract: Functionalized Organolithium Reagents. Part 10. Synthesis of Amines via Carbon-Sulfur Bond Cleavages of Substituted Aminomethyl Sulfides with Organolithium Reagents: Aminocarbene Route to Enamines and Sterically Hindered Amines. Cheminform. 25: no-no |