T. Novinson

发表

Synthesis and enzymic activity of some novel xanthine oxidase inhibitors. 3-Substituted 5,7-dihydroxypyrazolo(1,5-alpha)pyrimidines.

R. K. Robins, D. E. O'Brien, J. Miller, 1976, Journal of medicinal chemistry.

Synthesis and antischistosomal activity of certain pyrazolo[1,5-a]pyrimidines.

R. K. Robins, D. E. O'Brien, H. R. Wilson, 1975, Journal of medicinal chemistry.

3-Substituted 5,7-dimethylpyrazolo(1,5-a)pyrimidines, 3',5'-cyclic-AMP phosphodiesterase inhibitors. 1.

R. K. Robins, D. E. O'Brien, L. Simon, 1974, Journal of medicinal chemistry.

Adenosine cyclic 3',5',-monophosphate phosphodiesterasr inhibitors. 2.3-Substituted 5,7-dialkylpyrazolo [1,5-a]pyrimidines.

R. K. Robins, D. E. O'Brien, J. Miller, 1975, Journal of medicinal chemistry.

Dialkyl bicyclic heterocycles with a bridgehead nitrogen as purine analogs possessing significant cardiac inotropic activity: Dialkyl Bicyclic Heterocycles

R. K. Robins, T. Okabe, B. Bhooshan, 1983 .

2-(Alkylthio)-1,2,4-triazolo[1,5-a]pyrimidines as adenosine cyclic 3',5'-monophosphate phosphodiesterase inhibitors with potential as new cardiovascular agents.

R. K. Robins, D. E. O'Brien, J. Miller, 1982, Journal of Medicinal Chemistry.

A solution of structural ambiguity: s-Triazolo[1,5-a] – and s-triazolo[4.3-a] pyrimidines †

R. K. Robins, T. Okabe, P. Dea, 1975 .

3-Halo-5,7-dimethylpyrazolo [1,5-a]pyrimidines, a nonbenzodiazepinoid class of antianxiety agents devoid of potentiation of central nervous system depressant effects of ethanol or barbiturates.

R. K. Robins, T. Okabe, A. Dren, 1977, Journal of medicinal chemistry.

DIALKYL BICYCLIC HETEROCYCLES WITH A BRIDGEHEAD NITROGEN AS PURINE ANALOGS POSSESSING SIGNIFICANT CARDIAC INOTROPIC ACTIVITY

R. K. Robins, T. Okabe, B. Bhooshan, 1984 .

Mass spectra of substituted pyrazolo[1,5-a]-1,3,5-triazines

R. Foltz, K. Senga, H. E. Khadem, 1975 .

3‐SUBSTITUTED 5,7‐DIMETHYLPYRAZOLO(1,5‐A)PYRIMIDINES, 3′,5′‐CYCLIC‐AMP PHOSPHODIESTERASE INHIBITORS PART 1

R. K. Robins, D. E. O'Brien, L. Simon, 1974 .

Synthesis and antifungal properties of certain 7-alkylaminopyrazolo[1,5-a]pyrimidines.

R. K. Robins, T. Matthews, T. Novinson, 1977, Journal of medicinal chemistry.

ADENOSINE CYCLIC 3′,5′-MONOPHOSPHATE PHOSPHODIESTERASE INHIBITORS PART 2, 3-SUBSTITUTED 5,7-DIALKYLPYRAZOLO(1,5-A)PYRIMIDINES

R. K. Robins, Jon P. Miller, D. E. O'Brien, 1975 .

2-(ALKYLTHIO)-1,2,4-TRIAZOLO(1,5-A)PYRIMIDINES AS ADENOSINE 3′,5′-MONOPHOSPHATE PHOSPHODIESTERASE INHIBITORS WITH POTENTIAL AS NEW CARDIOVASCULAR AGENTS

R. K. Robins, Jon P. Miller, D. E. O'Brien, 1982 .

Synthesis of unsymmetrical 2,4-dialkylpyrazolo[1,5-a]-1,3,5-triazines

R. K. Robins, J. Kobe, D. E. O'Brien, 1974 .

Synthesis and antimicrobial activity of some novel heterocycles. Azolo-as-triazines.

R. K. Robins, T. Okabe, T. Matthews, 1976, Journal of medicinal chemistry.

The chemistry of 4-hydrazino-7-phenylpyrazolo[1,5-a] -1,3,5-triazines

Thomas Novinson, Roland K. Robins, R. K. Robins, 1974 .

Synthesis and enzymic activity of various substituted pyrazolo[1,5-a]-1,3,5-triazines as adenosine cyclic 3',5'-phosphate phosphodiesterase inhibitors.

R. K. Robins, D. E. O'Brien, J. Miller, 1982, Journal of medicinal chemistry.

Synthesis and enzymic activity of 6-carbethoxy- and 6-ethoxy-3,7-disubstituted-pyrazolo[1,5-a]pyrimidines and related derivatives as adenosine cyclic 3' ,5'-phosphate phosphodiesterase inhibitors.

R. K. Robins, D. E. O'Brien, J. Miller, 1982, Journal of medicinal chemistry.

The synthesis of certain 8-cyano-2,4-disubstituted-imidazo[1,5-a] pyrimidines

R. K. Robins, D. E. O'Brien, T. Novinson, 1974 .

Ring opening of 5,7-dimethyl-v-triazolo[1,5-a]pyrimidine by halogenating agents

T. Okabe, P. Dea, T. Novinson, 1976 .

Synthesis and antitrichomonal activity of certain pyrazolo (1,5-a) pyrimidines.

R. K. Robins, D. E. O'Brien, H. R. Wilson, 1975, Journal of medicinal chemistry.

NOVEL HETEROCYCLIC NITROFURFURAL HYDRAZONES. IN VIVO ANTITRYPANOSOMAL ACTIVITY

R. K. Robins, G. R. Revankar, T. Okabe, 1976 .