B. Savall

发表

Total synthesis of (-)-bafilomycin A(1).

M. Wendt, W. Roush, K. Scheidt, 2002, Journal of the American Chemical Society.

Identification of (R)-(2-Chloro-3-(trifluoromethyl)phenyl)(1-(5-fluoropyridin-2-yl)-4-methyl-6,7-dihydro-1H-imidazo[4,5-c]pyridin-5(4H)-yl)methanone (JNJ 54166060), a Small Molecule Antagonist of the P2X7 receptor.

T. Lovenberg, N. Carruthers, Hong Ao, 2016, Journal of medicinal chemistry.

Allyl-Assisted, Cu(I)-Catalyzed Azide-Alkyne Cycloaddition/Allylation Reaction: Assembly of the [1,2,3]Triazolo-4,5,6,7-tetrahydropyridine Core Structure.

C. Dvorak, B. Savall, J. Liang, 2015, The Journal of organic chemistry.

Synthesis, SAR, and Pharmacological Characterization of Brain Penetrant P2X7 Receptor Antagonists.

N. Carruthers, Hong Ao, A. Bhattacharya, 2015, ACS medicinal chemistry letters.

The evolution of P2X7 antagonists with a focus on CNS indications.

A. Bhattacharya, B. Savall, J. Rech, 2016, Bioorganic & medicinal chemistry letters.

4-Methyl-6,7-dihydro-4H-triazolo[4,5-c]pyridine-Based P2X7 Receptor Antagonists: Optimization of Pharmacokinetic Properties Leading to the Identification of a Clinical Candidate.

P. Bonaventure, C. Dvorak, T. Lovenberg, 2017, Journal of medicinal chemistry.

Preclinical characterization of substituted 6,7-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-8(5H)-one P2X7 receptor antagonists.

N. Carruthers, Hong Ao, A. Bhattacharya, 2016, Bioorganic & medicinal chemistry letters.

Discrete layers of ordered fullerene C60 molecules in the cocrystal C60.cntdot.CH2I2.cntdot.C6H6: synthesis, crystal structure, and carbon-13 NMR properties

Hsien‐Hau Wang, M. Whangbo, P. Mobley, 1992 .

Total synthesis of the formamicin aglycon, formamicinone.

W. Roush, B. Savall, N. Blanchard, 2003, Organic letters.

Identification of a potent, selective, and orally active leukotriene a4 hydrolase inhibitor with anti-inflammatory activity.

Cheryl A. Grice, Jianmei Wei, L. Karlsson, 2008, Journal of medicinal chemistry.

Tricyclic aminopyrimidine histamine H4 receptor antagonists.

Cheryl A. Grice, R. Thurmond, J. Edwards, 2011, Bioorganic & medicinal chemistry letters.

ChemInform Abstract: Highly Diastereoselective Synthesis of Propargylic 1,2-anti-Diol Derivatives Using α-Alkoxypropargylstannanes.

N. Powell, W. Roush, B. Savall, 2002 .

Total synthesis of formamicin.

N. Powell, W. Roush, B. Savall, 2004, Journal of the American Chemical Society.

Highly diastereoselective synthesis of propargylic 1,2-anti-diol derivatives using alpha-alkoxypropargylstannanes.

N. Powell, W. Roush, B. Savall, 2001, Organic letters.

Discovery and SAR of 6-alkyl-2,4-diaminopyrimidines as histamine H₄ receptor antagonists.

R. Thurmond, J. Edwards, M. Hack, 2014, Journal of medicinal chemistry.

A New Method for the Epoxidation of Alkenes in the Presence of Tertiary Amino Groups

B. Savall, W. Mcwhorter, D. Gleave, 1997 .

A New Method for the Epoxidation of Alkenes in the Presence of Tertiary Amino Groups.

B. Savall, W. Mcwhorter, D. Gleave, 1997 .

SYNTHESIS OF 6,7-DIHYDROXYOXINDOLE (A SUBUNIT OF PARAHERQUAMIDE A)

B. Savall, W. Mcwhorter, 1996 .

Clinical Development of Histamine H4 Receptor Antagonists.

Jennifer D. Venable, R. Thurmond, J. Edwards, 2017, Handbook of experimental pharmacology.

Total synthesis of the formamicin aglycon, formamicinone.

W. Roush, B. Savall, N. Blanchard, 2003, Organic letters.

Discovery of Imidazo[1,2-a]pyrazines and Pyrazolo[1,5-c]pyrimidines as TARP γ-8 Selective AMPAR Negative Modulators.

T. Lovenberg, N. Carruthers, B. Savall, 2018, ACS medicinal chemistry letters.

Lead Optimization of 5-Aryl Benzimidazolone- and Oxindole-Based AMPA Receptor Modulators Selective for TARP γ-8.

T. Lovenberg, N. Carruthers, B. Savall, 2018, ACS medicinal chemistry letters.

Discovery and Characterization of AMPA Receptor Modulators Selective for TARP-γ8

T. Lovenberg, N. Carruthers, T. Steckler, 2016, The Journal of Pharmacology and Experimental Therapeutics.

Identification of benzofuran central cores for the inhibition of leukotriene A(4) hydrolase.

Cheryl A. Grice, L. Karlsson, A. Fourie, 2013, Bioorganic & medicinal chemistry letters.

Superconductivity at 28.6 K in a rubidium-C60 fullerene compound, RbxC60, synthesized by a solution-phase technique

D. L. Overmyer, W. Kwok, S. Fleshler, 1991 .

First easily reproduced solution-phase synthesis and confirmation of superconductivity in the fullerene KxC60 (Tc = 18.0 ± 0.1 K)

W. Kwok, S. Fleshler, G. Crabtree, 1991 .

First Easily Reproduced Solution-Phase Synthesis and Confirmation of Superconductivity in the Fullerene KxC60 (Tc = 18.0 .+-. 0.1 K).

W. Kwok, S. Fleshler, D. Gruen, 1991 .

Superconductivity at 28.6 K in a Rubidium‐C60 Fullerene Compound, RbxC60, Synthesized by a Solution‐Phase Technique.

D. L. Overmyer, W. Kwok, S. Fleshler, 1991 .

Reply to “A Comment on ‘Discovery and Characterization of AMPA Receptor Modulators Selective for TARP-γ8’”

T. Lovenberg, N. Carruthers, B. Savall, 2016, The Journal of Pharmacology and Experimental Therapeutics.

Functional Profiling of 2-Aminopyrimidine Histamine H4 Receptor Modulators.

Jennifer D. Venable, R. Thurmond, B. Savall, 2015, Journal of medicinal chemistry.

Clinical Development of Histamine H4 Receptor Antagonists.

Jennifer D. Venable, R. Thurmond, J. Edwards, 2017, Handbook of experimental pharmacology.