29 results on '"Carpenter, Andrew J."'
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2. Stereoselective bromination of dehydroamino acids with controllable retention or inversion of olefin configuration
3. Development of Large-Scale Routes to Potent GPR119 Receptor Agonists
4. A convenient preparation of terminally differentiated, selectively protected six-carbon synthons from D-glucosamine
5. Synthesis of the aziridino(1,2-a)pyrrolidine substructure of the antitumor agents azinomycin A and
6. Facile reductive amination of aldehydes with electron-deficient anilines by acyloxyborohydrides in TFA: application to a diazaindoline scale-up
7. Discovery Process and Characterization of Novel Carbohydrazide Derivatives as Potent and Selective GHSR1a Antagonists
8. Discovery of Potent, Nonsystemic Apical Sodium-Codependent Bile Acid Transporter Inhibitors (Part 2)
9. Development of Large-Scale Routes to Potent GPR119 Receptor Agonists
10. Synthesis of the azabicyclic core of the azinomycins: introduction of differentiated trans-diol by crotylstannane addition to serinal
11. Discovery of 6,7-Dihydro-5H-pyrrolo[2,3-a]pyrimidines as Orally Available G Protein-Coupled Receptor 119 Agonists
12. Discovery Process and Characterization of Novel Carbohydrazide Derivatives as Potent and Selective GHSR1a Antagonists
13. 2,5-Disubstituted pyridines as potent GPR119 agonists
14. 1-Acetoxy-1,3-butadiene
15. Novel benzimidazole-based MCH R1 antagonists
16. Discovery of Potent, Nonsystemic Apical Sodium-Codependent Bile Acid Transporter Inhibitors (Part 1)
17. Discovery of Potent, Nonsystemic Apical Sodium-Codependent Bile Acid Transporter Inhibitors (Part 2)
18. Melanin-concentrating hormone receptor antagonists as potential antiobesity agents
19. 1-Acetoxy-1,3-butadiene
20. The chemistry-medicine continuum: Synthetic, computer, spectroscopic and biological studies on new chemotherapeutic leads
21. The development of strategies for construction of the aziridine core of the antitumor agents azinomycins A and B
22. Diastereoselective addition of vinyl organometallic reagents to l-serinal
23. Discovery of 6,7-Dihydro-5H-pyrrolo[2,3-a]pyrimidinesas OrallyAvailable G Protein-Coupled Receptor 119 Agonists.
24. Regioselective α- and β-metallations of thiophene derivatives bearing the 4,4-dimethyloxazolin-2-yl group. Application of the method to syntheses of 2,3- and 2,5-disubstituted thiophene derivatives.
25. The scope and limitations of carboxamide-induced .beta.-directed metalation of 2-substituted furan, thiophene, and 1-methylpyrrole derivatives. Application of the method to syntheses of 2,3-disubstituted thiophenes and furans
26. Chemoselective protection of heteroaromatic aldehydes as imidazolidine derivatives
27. Dimetallations of 2-substituted furans and thiophenes: approaches to the 2,3,5-trisubstituted heterocycles
28. High-yield syntheses of 2,3-disubstituted furans and thiophenes
29. High-yielding syntheses of 4(5)-substituted imidazoles via organolithium intermediates. the utility of sulphonamide n-protection and silicon-containing blocking groups
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