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T J Kress

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Advances in Heterocyclic Chemistry|January 1, 1970

The naphthyridinesW W Paudler, T J Kress

Journal of Chromatography|April 1, 1977

Thin-layer chromatographic separation of several chloro- and methyl-substituted 2-aminopyridinesI M Jakovljevic, R H Bishara, T J Kress

Annals of the New York Academy of Sciences|June 15, 1973

The selective dehalogenation of 2,4-dichloro-5(2,4-dichlorodiphenylmethyl)pyrimidineJ B Campbell, C W Whitehead, T J Kress, et al.

Journal of Medicinal Chemistry|August 1, 1987

Aromatase inhibition by 5-substituted pyrimidines and dihydropyrimidinesH M Taylor, C D Jones, J D Davenport, et al.

Journal of Medicinal Chemistry|March 26, 1999

Synthesis, pharmacological characterization, and molecular modeling of heterobicyclic amino acids related to (+)-2-aminobicyclo[3.1.0] hexane-2,6-dicarboxylic acid (LY354740): identification of two new potent, selective, and systemically active agonists for group II metabotropic glutamate receptorsJ A Monn, M J Valli, S M Massey, et al.

Pageof 1

Search research articles

Showing results (1-10 of 5) with videos related to

Sort By:

Pageof 1

Advances in Heterocyclic Chemistry|January 1, 1970

The naphthyridinesW W Paudler, T J Kress

Journal of Chromatography|April 1, 1977

Thin-layer chromatographic separation of several chloro- and methyl-substituted 2-aminopyridinesI M Jakovljevic, R H Bishara, T J Kress

Annals of the New York Academy of Sciences|June 15, 1973

The selective dehalogenation of 2,4-dichloro-5(2,4-dichlorodiphenylmethyl)pyrimidineJ B Campbell, C W Whitehead, T J Kress, et al.

Journal of Medicinal Chemistry|August 1, 1987

Aromatase inhibition by 5-substituted pyrimidines and dihydropyrimidinesH M Taylor, C D Jones, J D Davenport, et al.

Journal of Medicinal Chemistry|March 26, 1999

Synthesis, pharmacological characterization, and molecular modeling of heterobicyclic amino acids related to (+)-2-aminobicyclo[3.1.0] hexane-2,6-dicarboxylic acid (LY354740): identification of two new potent, selective, and systemically active agonists for group II metabotropic glutamate receptorsJ A Monn, M J Valli, S M Massey, et al.

Pageof 1