George A. Moniz - Concepedia

Author

George A. Moniz

Amgen (United States)

Also Known As

G. A. MONIZ, G. A. Moniz, G. Moniz, George A Moniz, George A. Moniz, George Moniz

Publications

838

Citations

H-Index

Concepts

All Affiliations

Amgen (United States)Yale University Swedish Orphan Biovitrum (Sweden)Eisai (United States)University of Massachusetts Dartmouth

About

George A. Moniz is an author at Amgen (United States) specializing in organic chemistry, engineering, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	9	9	322
2	Natural Sciences	6	6	283
3	Biomolecular Engineering	6	6	165
4	Medicine	4	4	254
5	Biochemistry	4	4	176

George A. Moniz

Publications

808

Citations

H-Index

Page 1

	Year	Citations
E7449: A dual inhibitor of PARP1/2 and tankyrase1/2 inhibits growth of DNA repair deficient tumors and antagonizes Wnt signaling Sharon McGonigle, Zhihong Chen, Jiayi Wu, Oncotarget Dual InhibitorGenome InstabilityOncologyTankyrase1/2 Inhibits GrowthMedicine	2015	84
Discovery of a Potent, Orally Active 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibitor for Clinical Study: Identification of (<i>S</i>)-2-((1<i>S</i>,2<i>S</i>,4<i>R</i>)-Bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5<i>H</i>)-one (AMG 221) Murielle M. Véniant, Clarence Hale, Randall W. Hungate, Journal of Medicinal Chemistry Molecular PharmacologyMedicinal ChemistryMethyl GroupBiochemistryC-5 Position	2010	80
Development of a Rhodium Carbenoid-Initiated Claisen Rearrangement for the Enantioselective Synthesis of α-Hydroxy Carbonyl Compounds John L. Wood, George A. Moniz, Derek A. Pflum, Journal of the American Chemical Society Chemical EngineeringCross-coupling ReactionEngineeringClaisen RearrangementAltmetric Attention Score	1999	74
An Aldol-Based Synthesis of (+)-Peloruside A, A Potent Microtubule Stabilizing Agent David A. Evans, Dennie S. Welch, Alexander W. H. Speed, Journal of the American Chemical Society	2009	67
Catalyst-Based Control of [2,3]- and [3,3]-Rearrangement in α-Diazoketone-Derived Propargyloxy Enols George A. Moniz, John L. Wood Journal of the American Chemical Society Cross-coupling ReactionEnantioselective SynthesisEngineeringDonut IconNatural Sciences	2001	62
A highly enantioselective catalyst for asymmetric hydroformylation of [2.2.1]-bicyclic olefins Jinkun Huang, Emilio E. Bunel, Alan M. Allgeier, Tetrahedron Letters Chemical EngineeringEngineeringAlkene MetathesisAsymmetric HydroformylationOrganic Chemistry	2005	55
A Baeyer-Villiger Oxidation Specifically Catalyzed by Human Flavin-Containing Monooxygenase 5 Wei‐Shiang Lai, Nadia Farah, George A. Moniz, Drug Metabolism and Disposition	2010	50
2-Amino-1,3-thiazol-4(5<i>H</i>)-ones as Potent and Selective 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibitors: Enzyme−Ligand Co-Crystal Structure and Demonstration of Pharmacodynamic Effects in C57Bl/6 Mice L. E. B. Johansson, Christopher Fotsch, Michael D. Bartberger, Journal of Medicinal Chemistry Pharmaceutical SciencePharmacotherapyEnzyme−ligand Co-crystal StructurePharmaceutical ChemistryMolecular Pharmacology	2008	49
Rhodium Carbenoid-Initiated Claisen Rearrangement: Scope and Mechanistic Observations John L. Wood, George A. Moniz Organic Letters	1999	48
Efficient Syntheses of (α-Fluoropropargyl)phosphonate Esters Farid Benayoud, Daniel J. deMendonca, Cheryl A. Digits, The Journal of Organic Chemistry Phosphonate Estersfarid BenayoudMedicinal ChemistryMolecular SciencesEngineeringNatural Sciences	1996	45

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