B. C. Bookser

发表

AMP deaminase inhibitors. 5. Design, synthesis, and SAR of a highly potent inhibitor series.

M. Erion, S. Kasibhatla, W. Xiao, 2001, Journal of medicinal chemistry.

Synthesis of 3′-Amino-3′-Deoxyguanosine and 3′-Amino-3′-Deoxyxyloguanosine Monophosphate Hepdirect Prodrugs from Guanosine

M. Erion, K. R. Reddy, B. C. Bookser, 2009, Nucleosides, nucleotides & nucleic acids.

Adenosine kinase inhibitors. 4. 6,8-Disubstituted purine nucleoside derivatives. Synthesis, conformation, and enzyme inhibition.

B. Ugarkar, Michael C. Matelich, B. C. Bookser, 2005, Journal of medicinal chemistry.

2-Benzyloxymethyl-5-(tributylstannyl)tetrazole. A reagent for the preparation of 5-aryl- and 5-heteroaryl-1H-tetrazoles via the Stille reaction†

B. C. Bookser, 2000 .

High-throughput five minute microwave accelerated glycosylation approach to the synthesis of nucleoside libraries.

B. C. Bookser, N. Raffaele, 2007, The Journal of organic chemistry.

AMP deaminase inhibitors. 3. SAR of 3-(carboxyarylalkyl)coformycin aglycon analogues.

M. Erion, S. Kasibhatla, J. Appleman, 2000, Journal of medicinal chemistry.

Syntheses of quadruply two- and three-atom, aza-bridged, cofacial bis(5,10,15,20-tetraphenylporphyrins)

T. C. Bruice, B. C. Bookser, 1991 .

Solvent-Controlled, Site-Selective N-Alkylation Reactions of Azolo-Fused Ring Heterocycles at N1-, N2-, and N3-Positions, Including Pyrazolo[3,4- d]pyrimidines, Purines, [1,2,3]Triazolo[4,5]pyridines, and Related Deaza-Compounds.

P. Stańczak, B. Dyck, A. Rheingold, 2018, The Journal of organic chemistry.

Synthesis and Acidity of 5-(m-Terphenyl-2'-yl)-1H-tetrazoles: Evidence for an Enhanced Polar-π Effect Compared to Carboxylic Acids.

K. Baldridge, J. Siegel, Yongsak Sritana-anant, 2021, Journal of medicinal chemistry.

2-Benzyloxymethyl-5-(tributylstannyl)tetrazole. A Reagent for the Preparation of 5-Aryl- and 5-Heteroaryl-1H-tetrazoles via the Stille Reaction.

B. C. Bookser, 2000 .

Azetidine-based selective glycine transporter-1 (GlyT1) inhibitors with memory enhancing properties.

Michael R. Kennedy, Kiev S. Ly, Marco Peters, 2020, Bioorganic & medicinal chemistry letters.

Total syntheses of (.+-.)-.alpha.- and (.+-.)-.beta.-copaene and formal total syntheses of (.+-.)-sativene, (.+-.)-cis-Sativenediol, and (.+-.)-helminthosporal

T. Arrhenius, E. Wenkert, B. C. Bookser, 1992 .

Design and Synthesis of Novel and Selective Glycine Transporter-1 (GlyT1) Inhibitors with Memory Enhancing Properties.

Michael R. Kennedy, Kiev S. Ly, D. M. Chung, 2018, Journal of medicinal chemistry.

Solid Phase Extraction Purification of Carboxylic Acid Products from 96-Well Format Solution Phase Synthesis with DOWEX 1×8-400 Formate Anion Exchange Resin

Shi-Yang Zhu, B. C. Bookser, 2001 .

AMP deaminase inhibitors. 2. Initial discovery of a non-nucleotide transition-state inhibitor series.

M. Erion, S. Kasibhatla, J. Appleman, 2000, Journal of medicinal chemistry.

Design and synthesis of the first potent, selective, and cell penetrating adenosine 5'-monophosphate deaminase inhibitors.

M. Erion, S. Kasibhatla, J. Appleman, 1998, Advances in experimental medicine and biology.

Adenosine kinase inhibitors. 6. Synthesis, water solubility, and antinociceptive activity of 5-phenyl-7-(5-deoxy-beta-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidines substituted at C4 with glycinamides and related compounds.

M. Erion, M. Allan, B. Ugarkar, 2005, Journal of medicinal chemistry.

DISCOVERY OF AMP MIMETICS THAT EXHIBIT HIGH INHIBITORY POTENCY AND SPECIFICITY FOR AMP DEAMINASE

M. Erion, S. Kasibhatla, J. Appleman, 1999 .

Synthesis of 3′-Amino-3′-deoxyguanosine and 3′-Amino-3′-deoxyxyloguanosine Monophosphate Hepdirect Prodrugs from Guanosine.

M. Erion, K. R. Reddy, B. C. Bookser, 2010 .