J. F. Gerster

发表

Imiquimod applied topically: a novel immune response modifier and new class of drug.

R. Miller, M. Tomai, H. Slade, 1999, International journal of immunopharmacology.

Cytokine induction by the immunomodulators imiquimod and S‐27609

T. Testerman, Richard L. Miller, M. Reiter, 1995, Journal of leukocyte biology.

Immunomodulating and antiviral activities of the imidazoquinoline S-28463.

R. Miller, M. Reiter, M. Tomai, 1995, Antiviral research.

Treatment of primary herpes simplex virus infection in guinea pigs by imiquimod.

R. Miller, Richard L. Miller, M. Reiter, 1999, Antiviral research.

Synthesis and structure-activity-relationships of 1H-imidazo[4,5-c]quinolines that induce interferon production.

Natalie J. Thompson, Richard L. Miller, M. Reiter, 2005, Journal of medicinal chemistry.

Structure of the nucleoside antibiotics formycin, formyein B and laurusin

R. K. Robins, Richard L. Miller, L. Townsend, 1966 .

Synthesis, absolute configuration, and antibacterial activity of 6,7-dihydro-5,8-dimethyl-9-fluoro-1-oxo-1H,5H- benzo[ij]quinolizine-2-carboxylic acid.

W. B. Gleason, J. F. Gerster, S. Pecore, 1987, Journal of medicinal chemistry.

PURINE NUCLEOSIDES. X. THE SYNTHESIS OF CERTAIN NATURALLY OCCURRING 2-SUBSTITUTED AMINO-9-BETA-D-RIBOFURANOSYLPURIN-6(1H)-ONES (N2-SUBSTITUTED GUANOSINES).

R. K. Robins, J. F. Gerster, 1965, Journal of the American Chemical Society.

Purine Nucleosides. IV. The Synthesis of 6-Halogenated 9-β-D-Ribofuranosylpurines from Inosine and Guanosine1

R. K. Robins, Jesse W. Jones, J. F. Gerster, 1963 .

Derivatives of the new ring system pyrazolo[4,3‐d]‐v‐triazine and the synthesis of 5,7‐disubstituted 3‐methylpyrazolo[4,3‐d] pyrimidines and 5,7‐disubstituted 3‐methylpyrazolo[4,3‐d]pyrimidine 6‐uxides which are structurally related to the nucleoside antibiotics formycin and formycin B

R. A. Long, L. Townsend, J. F. Gerster, 1970 .

Pyrrolopyrimidine nucleosides. IV. The synthesis of certain 4,5‐disubstituted‐7‐(β‐d‐ribofuranosyl)pyrrolo[2,3‐d]pyrimidines related to the pyrrolo[2,3‐d]pyrimidine nucleoside antibiotics

R. K. Robins, L. Townsend, J. F. Gerster, 1969 .

Antiinflammatory agents. I. 3-Benzoylfluoroalkanesulfonamides.

D. Kvam, R. Trancik, J. F. Gerster, 1970, Journal of medicinal chemistry.

Pyrrolopyrimidine nucleosides. V. A study on the relative chemical reactivity of the 5-cyano group of the nucleoside antibiotic toyocamycin and desaminotoyocamycin. The synthesis of analogs of sangivamycin.

R. K. Robins, L. Townsend, J. F. Gerster, 1970, The Journal of organic chemistry.

Differentiation of fluorinated quinolone antibacterials with Neisseria gonorrhoeae isolates.

J. F. Gerster, S. Pecore, S. Rohlfing, 1985, The Journal of antimicrobial chemotherapy.

Pyrrolopyrimidine Nucleosides. I. The Synthesis of 4-Substituted 7-(- D -Ribofuranosyl)pyrrolo[2,3-d]pyrimidines from Tubercidin.

R. K. Robins, L. Townsend, J. F. Gerster, 1967, Journal of medicinal chemistry.

A study of electrophilic substitution in the pyrrolo[2,3-d]pyrimidine ring†

R. K. Robins, L. Townsend, J. F. Gerster, 1969 .

Purine nucleosides. XIX. The synthesis of certain 8-chloropurine nucleosides and related derivatives.

R. K. Robins, L. Townsend, J. F. Gerster, 1968, The Journal of organic chemistry.

Potential Purine Antagonists. XXVIII. The Preparation of Various Bromopurines1

R. K. Robins, J. F. Gerster, A. Beaman, 1962 .

Disposition of radiolabeled flumequine in rat and dog.

L. Harrison, J. F. Gerster, R. Ober, 1986, Drug metabolism and disposition: the biological fate of chemicals.

Purine nucleosides. 8. The synthesis of 2-fluoro- and 2-chloroinosine and certain derived purine nucleosides.

R. K. Robins, J. F. Gerster, 1966, The Journal of organic chemistry.