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1. Report on the Family Support Act of 1988 Job Opportunities and Basic Skills (JOBS) Training Program.

2. Report on U.S. Department of Labor Programs and Funding through the Job Training Partnership Act (JTPA), 1990.

5. Discovery of BMS-753426: A Potent Orally Bioavailable Antagonist of CC Chemokine Receptor 2

6. Novel 1,4-homofragmentation via an [alpha]-lactone

7. Technetium(V) oxo complexes of substituted propylene diamine dioxime (PnAO) ligands: water-dependent interconversion between syn and anti isomers

12. Sulfonation with inversion by Mitsunobu reaction: an improvement on the original conditions

13. Regioselective coupling of tetraalkylammonium salts of 6-iodo-2-aminopurine to a cyclobutyl triflate: efficient preparation of homochiral BMS-180,194, a potent antiviral carbocyclic nucleoside

14. Peptidomimetic synthesis: A novel, highly stereoselective route to substituted freidinger lactams

15. Synthesis, characterization, and crystal structures of M(DO3A) (M = Fe, Gd) and Na(M(DOTA)) (M = Fe, Y, Gd)

16. Synthesis, characterization, and crystal structure of the gadolinium(III) chelate of (1R,4R,7R)-alpha,alpha',alpha''-trimethyl-1,4,7, 10-tetraazacyclododecane-1,4,7-triacetic acid (DO3MA)

17. The impact of long-term exercise training on psychological function in olderadults

18. The ratio of waist-to-hip circumference, plasma insulin level, and glucose intolerance as independent predictors of the HDL2 cholesterol level in older adults

20. Use of a Conformational-Switching Mechanism to Modulate Exposed Polarity: Discovery of CCR2 Antagonist BMS-741672

24. Language assessment of monolingual and multilingual children using non-word and sentence repetition tasks.

26. One-pot synthesis and conformational features of N,N'-distributed ketene animals

27. Identification of 1-{2-[4-chloro-1′-(2,2-dimethylpropyl)-7-hydroxy-1,2-dihydrospiro[indole-3,4′-piperidine]-1-yl]phenyl}-3-{5-chloro-[1,3]thiazolo[5,4-b]pyridin-2-yl}urea, a potent, efficacious and orally bioavailable P2Y1 antagonist as an antiplatelet agent

30. Utilization of a nitrogen–sulfur nonbonding interaction in the design of new 2-aminothiazol-5-yl-pyrimidines as p38α MAP kinase inhibitors

34. Novel Synthesis of the Hexahydroimidazo[1,5b]isoquinoline Scaffold: Application to the Synthesis of Glucocorticoid Receptor Modulators

37. Discovery of (R)-9-Ethyl-1,3,4,10b-tetrahydro-7-trifluoromethylpyrazino[2,1-a]isoindol- 6(2H)-one, a Selective, Orally Active Agonist of the 5-HT2C Receptor

38. Discovery of Potent, Orally-Active, and Muscle-Selective Androgen Receptor Modulators Based on an N-Aryl-hydroxybicyclohydantoin Scaffold

39. Discovery and Development of 5-[(5S,9R)-9- (4-Cyanophenyl)-3-(3,5-dichlorophenyl)-1- methyl-2,4-dioxo-1,3,7-triazaspiro[4.4]non- 7-yl-methyl]-3-thiophenecarboxylic Acid (BMS-587101)A Small Molecule Antagonist of Leukocyte Function Associated Antigen-1

44. Synthesis of Novel Potent Dipeptidyl Peptidase IV Inhibitors with Enhanced Chemical Stability: Interplay between the N-Terminal Amino Acid Alkyl Side Chain and the Cyclopropyl Group of α-Aminoacyl-l-cis-4,5-methanoprolinenitrile-Based Inhibitors

46. Molecular design and structure–Activity relationships leading to the potent, selective, and orally active thrombin active site inhibitor BMS-189664

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