Gerardo Byk

Affiliations: 
Bar Ilan University, Israel 
Area:
Nano-Biotechnology
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"Gerardo Byk"
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Publications

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Massarano T, Mazir A, Lavi R, et al. (2020) Solid-Phase Multicomponent Synthesis of 3-Substituted Isoindolinones Generates New Cell-Penetrating Probes as Drug Carriers. Chemmedchem. 15: 833-838
Turdiev A, Filiutovich O, Mirkin F, et al. (2019) A peptide from Testudo horsfieldii tortoise spleen as a potential helper for reducing acute radiation syndrome. Journal of Peptide Science : An Official Publication of the European Peptide Society. 25: e3202
Elhawi H, Eini H, Douvdevani A, et al. (2012) Improved methods for thermal rearrangement of alicyclic α-hydroxyimines to α-aminoketones: synthesis of ketamine analogues as antisepsis candidates. Molecules (Basel, Switzerland). 17: 6784-807
Khandadash R, Partouche S, Weiss A, et al. (2011) A Fully Synthetic “Phage-Like” System II: Synthesis and Live Cell Screening of Combinatorial Libraries of Peptides on Sub-Cellular Sized Microspheres The Open Optics Journal. 5: 17-27
Byk G, Partouche S, Weiss A, et al. (2010) Fully synthetic phage-like system for screening mixtures of small molecules in live cells. Journal of Combinatorial Chemistry. 12: 332-45
Mirkin F, Eini H, Douvdevani A, et al. (2009) New degradable cationic peptides for modulated gene delivery. Advances in Experimental Medicine and Biology. 611: 245-6
Byk G, Cohen-Ohana M, Raichman D. (2006) Fast and versatile microwave-assisted intramolecular Heck reaction in peptide macrocyclization using microwave energy. Biopolymers. 84: 274-82
Byk G, Kabha E. (2004) Anomalous regioselective four-member multicomponent Biginelli reaction II: one-pot parallel synthesis of spiro heterobicyclic aliphatic rings. Journal of Combinatorial Chemistry. 6: 596-603
Bitan G, Zeltser I, Byk G, et al. (1996) Backbone cyclization of the C-terminal part of substance P. Part 1: The important role of the sulphur in position 11. Journal of Peptide Science : An Official Publication of the European Peptide Society. 2: 261-9
Byk G, Halle D, Zeltser I, et al. (1996) Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogs of the C-terminal hexapeptide of substance P. Journal of Medicinal Chemistry. 39: 3174-8
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