2013 - Fellow of the American Chemical Society
1996 - Fellow of the American Association for the Advancement of Science (AAAS)
Her primary areas of investigation include Organic chemistry, Biochemistry, Stereochemistry, Reagent and Molecule. Her Organic chemistry study incorporates themes from Prodrug and Chemical synthesis. Her Biochemistry study integrates concerns from other disciplines, such as Tubulin, Microtubule and Cell biology.
Her Stereochemistry research incorporates themes from Combinatorial chemistry, Biological activity, Coupling and Enantioselective synthesis. Her Enantioselective synthesis research incorporates elements of Lactam, Side chain and Aldimine. Her research in Molecule intersects with topics in Amino acid, Nucleophile, Aqueous solution and Organic solvent.
The scientist’s investigation covers issues in Stereochemistry, Organic chemistry, Racism, Publishing and Public relations. Gunda I. Georg interconnects Biological activity, Chemical synthesis, Enantioselective synthesis and Cytotoxicity in the investigation of issues within Stereochemistry. Her research in Cytotoxicity focuses on subjects like Paclitaxel, which are connected to Microtubule.
Her work on Organic chemistry is being expanded to include thematically relevant topics such as Prodrug. Her Catalysis course of study focuses on Combinatorial chemistry and Palladium. Her research on In vitro concerns the broader Biochemistry.
Gunda I. Georg mainly focuses on Racism, Publishing, Public relations, Solidarity and Viewpoints. Racism combines with fields such as Environmental ethics and Chemistry in her investigation. Gunda I. Georg integrates many fields, such as Public relations, Commit, Diversity, Workforce and Inclusion, in her works.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
A convenient method for the efficient removal of ruthenium byproducts generated during olefin metathesis reactions.
Yu Mi Ahn;Kyoung Lang Yang;Gunda I. Georg.
Organic Letters (2001)
Efficient and practical asymmetric synthesis of the taxol C-13 side chain, N-benzoyl-(2R,3S)-3-phenylisoserine, and its analogs via chiral 3-hydroxy-4-aryl-.beta.-lactams through chiral ester enolate-imine cyclocondensation
Iwao Ojima;Ivan Habus;Mangzhu Zhao;Gunda I. Georg.
Journal of Organic Chemistry (1991)
Taxane Anticancer Agents Basic Science and Current Status
Gunda I. Georg;Thomas T. Chen;Iwao Ojima;Dolatrai M. Vyas.
A Preclinical Evaluation of Minnelide as a Therapeutic Agent Against Pancreatic Cancer
Rohit Chugh;Veena Sangwan;Satish P. Patil;Vikas Dudeja.
Science Translational Medicine (2012)
Hydrophobic collapse of taxol and taxotere solution conformations in mixtures of water and organic solvent
D. G. Vander Velde;G. I. Georg;G. L. Grunewald;C. W. Gunn.
Journal of the American Chemical Society (1993)
Mild and selective hydrozirconation of amides to aldehydes using Cp2Zr(H)Cl: scope and mechanistic insight.
Jared T. Spletstoser;Jonathan M. White;and Ashok Rao Tunoori;Gunda I. Georg.
Journal of the American Chemical Society (2007)
Palladium(II)-catalyzed direct arylation of enaminones using organotrifluoroborates.
Haibo Ge;Micah J. Niphakis;Gunda I. Georg.
Journal of the American Chemical Society (2008)
Acetyl-lysine Binding Site of Bromodomain-Containing Protein 4 (BRD4) Interacts with Diverse Kinase Inhibitors.
Stuart W.J. Ember;Jin Yi Zhu;Sanne H. Olesen;Mathew P. Martin.
ACS Chemical Biology (2014)
Synthesis of biologically active taxol analogues with modified phenylisoserine side chains.
Gunda I. Georg;Zacharia S. Cheruvallath;Richard H. Himes;Magdalena R. Mejillano.
Journal of Medicinal Chemistry (1992)
Asymmetric synthesis of (1′R,3R,4R)-4-acetoxy-3-(1′-((tert-butyldimethylsilyl)oxy)ethyl)-2- azetidinone and other 3-(1′-Hydroxyethyl)-2-azetidinones from (S)-(+)-Ethyl 3-hydroxybutanoate: Formal total synthesis of (+)-thienamycin
Gunda I. Georg;Joydeep Kant;Harpal S. Gill.
Journal of the American Chemical Society (1987)
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