Peter G. Dormer - Concepedia

Author

Peter G. Dormer

Merck & Co., Inc., Rahway, NJ, USA (United States)

Also Known As

Dormer, P.G., Dormer, Peter G., P Dormer, P Dörmer, P. Dormer, P. DÖRMER, P. Dörmer, P. Dörmér, P. G. DORMER, P. G. Dormer

296

Publications

6.3K

Citations

H-Index

138

Concepts

All Affiliations

Merck & Co., Inc., Rahway, NJ, USA (United States)Munich Security Conference Institut für Umwelttechnologien und Strahlenschutz (Germany)Institut für Hämatopathologie Hamburg

About

Peter G. Dormer is an author at Merck & Co., Inc., Rahway, NJ, USA (United States) specializing in chemistry, organic chemistry, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	43	1.7K
2	Engineering	20	26	1.7K
3	Natural Sciences	17	31	1.4K
4	Health Sciences	10	10	368
5	Language Studies	2	2	43

Peter G. Dormer

113

Publications

5.6K

Citations

H-Index

Page 1

	Year	Citations
Mast cell growth‐enhancing activity (MEA) is structurally related and functionally identical to the novel mouse T cell growth factor P40/TCGFIII (interleukin 9) Lothar Hültner, C Druez, J Moeller, European Journal of Immunology	1990	303
Ullmann Diaryl Ether Synthesis: Rate Acceleration by 2,2,6,6-Tetramethylheptane-3,5-dione Elizabeth Buck, Zhiguo J. Song, David M. Tschaen, Organic Letters Cesium CarbonateChemical EngineeringCross-coupling ReactionEngineeringDifficult Reaction	2002	294
Enantioselective, Palladium-Catalyzed α-Arylation of <i>N</i>-Boc-pyrrolidine Kevin R. Campos, Artis Klapars, Jacob H. Waldman, Journal of the American Chemical Society	2006	273
Efficient and General Protocol for the Copper-Free Sonogashira Coupling of Aryl Bromides at Room Temperature Arash Soheili, Jennifer Albaneze‐Walker, Jerry A. Murry, Organic Letters Room TemperatureCross-coupling ReactionGeneral ProtocolEngineeringPhysics	2003	262
Efficient Cross-Coupling of Secondary Alkyltrifluoroborates with Aryl Chlorides—Reaction Discovery Using Parallel Microscale Experimentation Spencer D. Dreher, Peter G. Dormer, Deidre L. Sandrock, Journal of the American Chemical Society	2008	260
Efficient Synthesis of NK<sub>1</sub> Receptor Antagonist Aprepitant Using a Crystallization-Induced Diastereoselective Transformation Karel M. J. Brands, Joseph F. Payack, Jonathan D. Rosen, Journal of the American Chemical Society Medicinal ChemistryBiochemistryFunctional SelectivityLewis AcidReceptor Antagonist Aprepitant	2003	156
Highly Regioselective Friedländer Annulations with Unmodified Ketones Employing Novel Amine Catalysts: Syntheses of 2-Substituted Quinolines, 1,8-Naphthyridines, and Related Heterocycles Peter G. Dormer, Kan K. Eng, Roger N. Farr, The Journal of Organic Chemistry Chemical EngineeringEngineeringHeterocyclicRegioselective Friedländer AnnulationsOxide Catalysts	2002	132
Synthesis of Benzo[<i>b</i>]furans via CuI-Catalyzed Ring Closure Cheng‐Yi Chen, Peter G. Dormer The Journal of Organic Chemistry Wide VarietyEngineeringHeterocyclicCui-catalyzed Ring ClosureOrganic Chemistry	2005	130
Cell kinetics in human malignancies studied with in vivo administration of bromodeoxyuridine and flow cytometry. Alberto Riccardi, Marco Danova, George D. Wilson, PubMed Mixed-phenotype Acute LeukemiaBrdurd Infusion MethodPathologyTumor BiologyMyeloid Neoplasia	1988	127
A Mild and Efficient Synthesis of 4-Quinolones and Quinolone Heterocycles Daniel Zewge, Cheng‐yi Chen, Curtis Deer, The Journal of Organic Chemistry Cyclization ProtocolEngineeringHeterocyclicMedicineOrganic Chemistry	2007	121

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