Gunda Georg
Gunda Georg
Professor of Medicinal Chemistry, University of Minnesota
Verified email at - Homepage
Cited by
Cited by
The organic chemistry of β-lactams
GI Georg
(No Title), 1993
A convenient method for the efficient removal of ruthenium byproducts generated during olefin metathesis reactions
YM Ahn, KL Yang, GI Georg
Organic Letters 3 (9), 1411-1413, 2001
The ecstasy and agony of assay interference compounds
C Aldrich, C Bertozzi, GI Georg, L Kiessling, C Lindsley, D Liotta, ...
ACS Chemical Neuroscience 8 (3), 420-423, 2017
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 …
I Ojima, I Habus, M Zhao, GI Georg, LR Jayasinghe
The Journal of Organic Chemistry 56 (5), 1681-1683, 1991
A preclinical evaluation of Minnelide as a therapeutic agent against pancreatic cancer
R Chugh, V Sangwan, SP Patil, V Dudeja, RK Dawra, S Banerjee, ...
Science translational medicine 4 (156), 156ra139-156ra139, 2012
Mild and Selective Hydrozirconation of Amides to Aldehydes Using Cp2Zr(H)Cl:  Scope and Mechanistic Insight
JT Spletstoser, JM White, AR Tunoori, GI Georg
Journal of the American Chemical Society 129 (11), 3408-3419, 2007
Acetyl-lysine binding site of bromodomain-containing protein 4 (BRD4) interacts with diverse kinase inhibitors
SWJ Ember, JY Zhu, SH Olesen, MP Martin, A Becker, N Berndt, GI Georg, ...
ACS chemical biology 9 (5), 1160-1171, 2014
" hydrophobic collapse" of taxol and Taxotere solution conformations in mixtures of water and organic solvent
DG Vander Velde, GI Georg, GL Grunewald, CW Gunn, LA Mitscher
Journal of the American Chemical Society 115 (24), 11650-11651, 1993
Discovery of a potential allosteric ligand binding site in CDK2
S Betzi, R Alam, M Martin, DJ Lubbers, H Han, SR Jakkaraj, GI Georg, ...
ACS chemical biology 6 (5), 492-501, 2011
A Novel and Expeditious Reduction of Tertiary Amides to Aldehydes Using Cp2Zr(H)Cl
JM White, AR Tunoori, GI Georg
Journal of the American Chemical Society 122 (48), 11995-11996, 2000
Palladium (II)-catalyzed direct arylation of enaminones using organotrifluoroborates
H Ge, MJ Niphakis, GI Georg
Journal of the American Chemical Society 130 (12), 3708-3709, 2008
Synthesis of biologically active taxol analogs with modified phenylisoserine side chains
GI Georg, ZS Cheruvallath, RH Himes, MR Mejillano, CT Burke
Journal of medicinal chemistry 35 (22), 4230-4237, 1992
Taxane anticancer agents: basic science and current status
GI Georg, TT Chen, I Ojima, DM Vyas
American Chemical Society, 1994
Cyclin-dependent kinase inhibitor dinaciclib interacts with the acetyl-lysine recognition site of bromodomains
MP Martin, SH Olesen, GI Georg, E Schönbrunn
ACS chemical biology 8 (11), 2360-2365, 2013
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 …
GI Georg, J Kant, HS Gill
Journal of the American Chemical Society 109 (4), 1129-1135, 1987
Epothilone and paclitaxel: unexpected differences in promoting the assembly and stabilization of yeast microtubules
CJ Bode, ML Gupta, EA Reiff, KA Suprenant, GI Georg, RH Himes
Biochemistry 41 (12), 3870-3874, 2002
Polymer-bound triphenylphosphine as traceless reagent for Mitsunobu reactions in combinatorial chemistry: Synthesis of aryl ethers from phenols and alcohols
AR Tunoori, D Dutta, GI Georg
Tetrahedron letters 39 (48), 8751-8754, 1998
The cryptophycins: their synthesis and anticancer activity
MJ Eggen, GI Georg
Medicinal research reviews 22 (2), 85-101, 2002
β-Amyloid-induced neurodegeneration and protection by structurally diverse microtubule-stabilizing agents
ML Michaelis, S Ansar, Y Chen, ER Reiff, KI Seyb, RH Himes, KL Audus, ...
Journal of Pharmacology and Experimental Therapeutics 312 (2), 659-668, 2005
Understanding tubulin–Taxol interactions: mutations that impart Taxol binding to yeast tubulin
ML Gupta Jr, CJ Bode, GI Georg, RH Himes
Proceedings of the National Academy of Sciences 100 (11), 6394-6397, 2003
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