Adelina Voutchkova-Kostal, Ph.D. - Publications

Affiliations: 
2012- Chemistry George Washington University, Washington, DC, United States 
Area:
organometallics, catalysis, green chemistry
Website:
https://blogs.gwu.edu/avoutchkova/

28 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Kostal J, Voutchkova-Kostal A. Going All In: A Strategic Investment in Toxicology. Chemical Research in Toxicology. PMID 32166946 DOI: 10.1021/acs.chemrestox.9b00497  0.32
2020 Heltzel JM, Finn M, Ainembabazi D, Wang K, Voutchkova-Kostal AM. Correction: Transfer hydrogenation of carbon dioxide and bicarbonate from glycerol under aqueous conditions. Chemical Communications (Cambridge, England). PMID 32096808 DOI: 10.1039/d0cc90084b  0.72
2019 Ainembabazi D, Reid C, Chen A, An N, Kostal J, Voutchkova-Kostal A. Decarbonylative olefination of aldehydes to alkenes. Journal of the American Chemical Society. PMID 31884790 DOI: 10.1021/jacs.9b12354  1
2019 Mills MG, Ramsden R, Ma EY, Corrales J, Kristofco LA, Steele WB, Saari GN, Melnikov F, Kostal J, Kavanagh TJ, Zimmerman JB, Voutchkova-Kostal AM, Brooks BW, Coish P, Anastas PT, et al. CRISPR-generated Nrf2a loss- and gain-of-function mutants facilitate mechanistic analysis of chemical oxidative stress-mediated toxicity in zebrafish. Chemical Research in Toxicology. PMID 31858786 DOI: 10.1021/acs.chemrestox.9b00346  0.72
2019 Steele WB, Kristofco LA, Corrales J, Saari GN, Corcoran EJ, Hill BN, Mills MG, Gallagher E, Kavanagh TJ, Melnikov F, Zimmerman JB, Voutchkova-Kostal AM, Anastas PT, Kostal J, Brooks BW. Towards less hazardous industrial compounds: coupling quantum mechanical computations, biomarker responses and behavioral profiles identify bioactivity of SN2 electrophiles in alternative vertebrate models. Chemical Research in Toxicology. PMID 31789507 DOI: 10.1021/acs.chemrestox.9b00290  0.72
2019 An N, Ainembabazi D, Reid C, Samudrala K, Wilson K, Lee AF, Voutchkova-Kostal A. Microwave-assisted decarbonylation of biomass-derived aldehydes using Pd-doped hydrotalcites. Chemsuschem. PMID 31595700 DOI: 10.1002/cssc.201901934  1
2018 Steele WB, Kristofco LA, Corrales J, Saari GN, Haddad SP, Gallagher EP, Kavanagh TJ, Kostal J, Zimmerman JB, Voutchkova-Kostal A, Anastas P, Brooks BW. Comparative behavioral toxicology with two common larval fish models: Exploring relationships among modes of action and locomotor responses. The Science of the Total Environment. 640: 1587-1600. PMID 30021323 DOI: 10.1016/j.scitotenv.2018.05.402  0.56
2018 Heltzel JM, Finn M, Ainembabazi D, Wang K, Voutchkova-Kostal AM. Transfer hydrogenation of carbon dioxide and bicarbonate from glycerol under aqueous conditions. Chemical Communications (Cambridge, England). PMID 29845981 DOI: 10.1039/c8cc03157f  0.72
2017 Coish P, Brooks BW, Gallagher EP, Mills M, Kavanagh TJ, Simcox N, Lasker GA, Botta D, Schmuck SC, Voutchkova-Kostal A, Kostal J, Mullins ML, Nesmith SM, Mellor KE, Corrales J, et al. The Molecular Design Research Network: An Overview. Toxicological Sciences : An Official Journal of the Society of Toxicology. PMID 28973416 DOI: 10.1093/toxsci/kfx175  0.72
2016 Corrales J, Kristofco LA, Steele WB, Saari GN, Kostal J, Williams ES, Mills M, Gallagher EP, Kavanagh TJ, Simcox N, Shen LQ, Melnikov F, Zimmerman JB, Voutchkova-Kostal AM, Anastas PT, et al. Towards the design of less hazardous chemicals: Exploring comparative oxidative stress in two common animal models. Chemical Research in Toxicology. PMID 27750016 DOI: 10.1021/acs.chemrestox.6b00246  0.72
2015 Kostal J, Voutchkova-Kostal AM. CADRE-SS, an in silico tool for predicting skin sensitization potential based on modeling of molecular interactions. Chemical Research in Toxicology. PMID 26650775 DOI: 10.1021/acs.chemrestox.5b00392  0.32
2015 Kostal J, Voutchkova-Kostal A, Anastas PT, Zimmerman JB. Identifying and designing chemicals with minimal acute aquatic toxicity. Proceedings of the National Academy of Sciences of the United States of America. 112: 6289-94. PMID 24639521 DOI: 10.1073/pnas.1314991111  0.72
2014 An N, Van Der Mei F, Voutchkova-Kostal A. Global Model for Octanol-Water Partition Coefficients from Proton Nuclear Magnetic Resonance Spectra. Molecular Informatics. 33: 286-92. PMID 27485775 DOI: 10.1002/minf.201300172  1
2014 Connors KA, Voutchkova-Kostal AM, Kostal J, Anastas P, Zimmerman JB, Brooks BW. Reducing aquatic hazards of industrial chemicals: probabilistic assessment of sustainable molecular design guidelines. Environmental Toxicology and Chemistry / Setac. 33: 1894-902. PMID 24839109 DOI: 10.1002/etc.2614  0.56
2012 Kostal J, Voutchkova-Kostal A, Weeks B, Zimmerman JB, Anastas PT. A free energy approach to the prediction of olefin and epoxide mutagenicity and carcinogenicity. Chemical Research in Toxicology. 25: 2780-7. PMID 23106682 DOI: 10.1021/tx300402b  0.72
2012 Kostal J, Voutchkova AM, Jorgensen WL. Investigation of solvent effects on the rate and stereoselectivity of the Henry reaction. Organic Letters. 14: 260-3. PMID 22168236 DOI: 10.1021/ol2030394  0.92
2012 Voutchkova-Kostal AM, Kostal J, Connors KA, Brooks BW, Anastas PT, Zimmerman JB. Towards rational molecular design for reduced chronic aquatic toxicity Green Chemistry. 14: 1001-1008. DOI: 10.1039/c2gc16385c  0.72
2011 Voutchkova AM, Kostal J, Steinfeld JB, Emerson JW, Brooks BW, Anastas P, Zimmerman JB. Towards rational molecular design: Derivation of property guidelines for reduced acute aquatic toxicity Green Chemistry. 13: 2373-2379. DOI: 10.1039/c1gc15651a  0.92
2011 Lapkin AA, Voutchkova A, Anastas P. A conceptual framework for description of complexity in intensive chemical processes Chemical Engineering and Processing: Process Intensification. 50: 1027-1034. DOI: 10.1016/j.cep.2011.06.005  0.92
2010 Voutchkova AM, Osimitz TG, Anastas PT. Toward a comprehensive molecular design framework for reduced hazard. Chemical Reviews. 110: 5845-82. PMID 20873708 DOI: 10.1021/cr9003105  0.92
2010 Voutchkova AM, Ferris LA, Zimmerman JB, Anastas PT. Toward molecular design for hazard reduction-fundamental relationships between chemical properties and toxicity Tetrahedron. 66: 1031-1039. DOI: 10.1016/j.tet.2009.11.002  0.92
2009 Voutchkova AM, Crabtree RH. Iridium-catalyzed benzylic C-H activation and functionalization of alkyl arenes Journal of Molecular Catalysis a: Chemical. 312: 1-6. DOI: 10.1016/j.molcata.2009.07.019  0.92
2008 Voutchkova A, Coplin A, Leadbeater NE, Crabtree RH. Palladium-catalyzed decarboxylative coupling of aromatic acids with aryl halides or unactivated arenes using microwave heating. Chemical Communications (Cambridge, England). 6312-4. PMID 19048139 DOI: 10.1039/b813998a  0.92
2008 Voutchkova AM, Gnanamgari D, Jakobsche CE, Butler C, Miller SJ, Parr J, Crabtree RH. Selective partial reduction of quinolines: Hydrosilylation vs. transfer hydrogenation Journal of Organometallic Chemistry. 693: 1815-1821. DOI: 10.1016/j.jorganchem.2008.02.004  0.92
2007 Voutchkova AM, Feliz M, Clot E, Eisenstein O, Crabtree RH. Imidazolium carboxylates as versatile and selective N-heterocyclic carbene transfer agents: synthesis, mechanism, and applications. Journal of the American Chemical Society. 129: 12834-46. PMID 17900114 DOI: 10.1021/ja0742885  0.92
2007 Leung CH, Voutchkova AM, Crabtree RH, Balcells D, Eisenstein O. Atom economic synthesis of amides via transition metal catalyzed rearrangement of oxaziridines Green Chemistry. 9: 976-979. DOI: 10.1039/b706164a  0.92
2005 Voutchkova AM, Appelhans LN, Chianese AR, Crabtree RH. Disubstituted imidazolium-2-carboxylates as efficient precursors to N-heterocyclic carbene complexes of Rh, Ru, Ir, and Pd. Journal of the American Chemical Society. 127: 17624-5. PMID 16351090 DOI: 10.1021/ja056625k  0.92
2005 Choi S, Cooley RB, Voutchkova A, Leung CH, Vastag L, Knowles DE. Oxidation of guanosine derivatives by a platinum(IV) complex: internal electron transfer through cyclization. Journal of the American Chemical Society. 127: 1773-81. PMID 15701012 DOI: 10.1021/ja045194n  0.92
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