Yayınlar

Synthesis, Characterization and End-Functionalization of a Novel Telechelic Star: Styrene Hexamer Core Carrying Polyisobutylene Arms Fitted with Allyl Termini
Synthesis, Characterization and End-Functionalization of a Novel Telechelic Star: Styrene Hexamer Core Carrying Polyisobutylene Arms Fitted with Allyl Termini
Kennedy, J., Nugay, T., Nugay, N. Polymer Bulletin , 5697 , Impact Factor: 1.660 , Q2 2020
Alendronate-functionalized poly(amido amine) cryogels of high-toughness for biomedical applications
Alendronate-functionalized poly(amido amine) cryogels of high-toughness for biomedical applications
Guven, M. N., Demirci, G., Altuncu, S., Gulyuz, U., Okay, O., Yagci Acar, H., Avci, D. Polymer , 190 , 122248 , Impact Factor: 3.771 , Q1 2020
Water soluble polymeric photoinitiator for dual-curing of acrylates and methacrylates
Water soluble polymeric photoinitiator for dual-curing of acrylates and methacrylates
Eren, T. N., Lalevee, J., Avci, D. Journal of Photochemistry and Photobiology A: Chemistry , 389 , 112288 , Impact Factor: 3.261 , Q2 2020
Synthesis of thiazol‐2‐imines from the reduction of single enantiomer 2‐imino‐thiazolidin‐4‐ones followed by a spontaneous water elimination
Synthesis of thiazol‐2‐imines from the reduction of single enantiomer 2‐imino‐thiazolidin‐4‐ones followed by a spontaneous water elimination
Teke Tuncel, S., Dogan, I. Chirality , 32 , 866-875 , Impact Factor: 1.910 , Q2 2020
Solvent Effects on Thiol−Ene Kinetics and Reactivity of Carbon and Sulfur Radicals
Solvent Effects on Thiol−Ene Kinetics and Reactivity of Carbon and Sulfur Radicals
Munar, I., Findik, V., Degirmenci, Aviyente, V. Journal of Physical Chemistry A , 124 (13) , 2580-1590 , Impact Factor: 2.634 , Q2 2020
Local Vibrational Mode Analysis of Ion-Solvent and Solvent-Solvent Interactions for Hydrated Ca2+ Clusters
Local Vibrational Mode Analysis of Ion-Solvent and Solvent-Solvent Interactions for Hydrated Ca2+ Clusters
Delgado, A., Sethio, D., Munar, I., Aviyente, V., Kraka, E. Journal of Chemical Physics , 153 (22) , 224303 , Impact Factor: 2.997 , Q1 2020
Elucidation of the Atroposelectivity in the Synthesis of Axially Chiral Thiohydantoin Derivatives
Elucidation of the Atroposelectivity in the Synthesis of Axially Chiral Thiohydantoin Derivatives
Haslak, Z. P., Cinar Agopcan, S., Ozbek Sarigul, Monard, G., Dogan, I., Aviyente, V. Organic & Biomolecular Chemistry , 18 , 2233-2241 , Impact Factor: 3.274 , Q1 2020
Micropatterned Reactive Nanofibers: Facile Fabrication of a Versatile Biofunctionalizable Interface
Micropatterned Reactive Nanofibers: Facile Fabrication of a Versatile Biofunctionalizable Interface
Kalaoglu-Altan, O.I., Sanyal, R., Sanyal, A. ACS Applied Polymer Materials , 2 (9) , 4026-4036 2020
Fabrication of Patterned Hydrogel Interfaces: Exploiting the Maleimide Group as a Dual Purpose Handle for Cross-Linking and Bioconjugation
Fabrication of Patterned Hydrogel Interfaces: Exploiting the Maleimide Group as a Dual Purpose Handle for Cross-Linking and Bioconjugation
Cengiz, N., Gevrek, T. N., Sanyal, R., Sanyal, A. Bioconjugate Chemistry , 31 (5) , 1382-1391 , Impact Factor: 4.031 , Q1 2020
Axially Chiral Hemiaminals From Nonracemic α‐amino Acid Derivatives (Thiohydantoins): Synthesis And Isomer Identification
Axially Chiral Hemiaminals From Nonracemic α‐amino Acid Derivatives (Thiohydantoins): Synthesis And Isomer Identification
Sarigul Ozbek, S., Dogan, I. Chirality , 32 , 1299-1310 , Impact Factor: 1.910 , Q2 2020
Trastuzumab targeted micellar delivery of docetaxel using dendron-polymer conjugates
Trastuzumab targeted micellar delivery of docetaxel using dendron-polymer conjugates
Bolu, B. S., Golba, B., Sanyal, A., Sanyal, R. Biomaterials Science (RSC) , 8 (9) , 2600-2610 , Impact Factor: 6.183 , Q1 2020
A Blind SAMPL6 Challenge: Insight Into the Octanol-Water Partition Coefficients of Drug-Like Molecules via a DFT Approach
A Blind SAMPL6 Challenge: Insight Into the Octanol-Water Partition Coefficients of Drug-Like Molecules via a DFT Approach
Arslan, E., Findik, B.K., Aviyente, V. Journal of Computer Aided Molecular Design , 34 , 463-470 , Impact Factor: 3.583 , Q2 2020