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3. Discovery of 3-Cyano-N-(3-(1-isobutyrylpiperidin-4-yl)-1-methyl-4-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl)benzamide: A Potent, Selective, and Orally Bioavailable Retinoic Acid Receptor-Related Orphan Receptor C2 Inverse Agonist

4. Identification of N-{cis-3-[Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl}propane-1-sulfonamide (PF-04965842): A Selective JAK1 Clinical Candidate for the Treatment of Autoimmune Diseases

5. Total synthesis of enantiopure phalarine via a stereospecific Pictet-Spengler reaction: traceless transfer of chirality from L-tryptophan

6. Total synthesis of complestatin: development of a Pd(0)-mediated indole annulation for macrocyclization

7. Total synthesis of chloropeptin II (complestatin) and chloropeptin I

8. Toward homogeneous erythropoietin: chemical synthesis of the [Ala.sup.sup.1]-[Gly.sup.28] glycopeptide domain by 'alanine' ligation

9. A unique class of duocarmycin and CC-1065 analogues subject to reductive activation

10. Systematic exploration of the structural features of yatekemycin impacting DNA alkylation and biological activity

11. Discovery of Clinical Candidate 1-{[(2S,3S,4S)-3-Ethyl-4-fluoro-5-oxopyrrolidin-2-yl]methoxy}-7-methoxyisoquinoline-6-carboxamide (PF-06650833), a Potent, Selective Inhibitor of Interleukin-1 Receptor Associated Kinase 4 (IRAK4), by Fragment-Based Drug Design

12. Selective targeting of the BRG/PB1 bromodomains impairs embryonic and trophoblast stem cell maintenance

13. Identification of N-{cis-3-[Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl}propane-1-sulfonamide (PF-04965842): A Selective JAK1 Clinical Candidate for the Treatment of Autoimmune Diseases

14. Identification of a Chemical Probe for Family VIII Bromodomains through Optimization of a Fragment Hit

17. Identification of a Chemical Probe for Bromo and Extra C-Terminal Bromodomain Inhibition through Optimization of a Fragment-Derived Hit

27. Identification of a ChemicalProbe for Bromo and ExtraC-Terminal Bromodomain Inhibition through Optimization of aFragment-Derived Hit.

28. Toward Homogeneous Erythropoietin: Chemical Synthesis of the Ala1 —Gly28 Glycopeptide Domain by "Alanine" Ligation.

29. Asymmetric Total Synthesis of (+)- and ent-()-Yatakemycin and Duocarmycin SA: Evaluation of Yatakemycin Key Partial Structures and Its Unnatural Enantiomer.

30. Discovery of 3-Cyano- N-(3-(1-isobutyrylpiperidin-4-yl)-1-methyl-4-(trifluoromethyl)-1 H-pyrrolo[2,3- b]pyridin-5-yl)benzamide: A Potent, Selective, and Orally Bioavailable Retinoic Acid Receptor-Related Orphan Receptor C2 Inverse Agonist.

31. A novel achiral seco-amino-cyclopropylindoline (CI) analog of CC-1065 and the duocarmycins: design, synthesis and biological studies.

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