Elisey Yagodkin, Ph.D.

Affiliations: 
2010 Chemistry University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
Organic Chemistry; Materials Chemistry
Google:
"Elisey Yagodkin"
Mean distance: 8.04
 
SNBCP

Parents

Sign in to add mentor
Christopher J. Douglas grad student 2010 UMN
 (Electrical properties and synthesis of tetracene and rubrene derivatives.)
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Gu X, Luhman WA, Yagodkin E, et al. (2012) Diarylindenotetracenes via a selective cross-coupling/C-H functionalization: electron donors for organic photovoltaic cells. Organic Letters. 14: 1390-3
Yagodkin E, McGarry KA, Douglas CJ. (2011) Preparation of 6,11-dihydroxy-5,12-tetracenedione Organic Preparations and Procedures International. 43: 360-363
Gu X, Luhman WA, Yagodkin E, et al. (2011) Synthesis and photovoltaic application of diarylindenotetracenes from a cross-coupling/C-H activation cascade reaction of peri-substituted tetrachlorotetracene Acs National Meeting Book of Abstracts
Yagodkin E, Douglas CJ. (2010) Low temperature Kumada-Corriu cross-coupling of polychlorinated acene derivatives and a synthesis of sterically demanding acenes Tetrahedron Letters. 51: 3037-3040
Yagodkin E, Xia Y, Kalihari V, et al. (2009) Synthesis, solid state properties, and semiconductor measurements of 5,6,11,12-tetrachlorotetracene Journal of Physical Chemistry C. 113: 16544-16548
Smit WA, Yagodkin EA, Zatonsky GV. (2005) Reactions of p-toluenesulfenyl chloride with enol acetates. The synthetic potential of the resulting adducts Russian Chemical Bulletin. 54: 743-747
Smit WA, Gromov AV, Yagodkin EA. (2003) Adducts of ArSCl with vinyl ethers or esters as synthones in geminal alkylation Mendeleev Communications. 13: 21-23
Tomilov YV, Kostyuchenko IV, Okonnishnikova GP, et al. (2000) Reactions of spirocyclopropane-containing 1- and 2-pyrazolines with electrophilic reagents Russian Chemical Bulletin. 49: 472-477
See more...