Robert W. Morrison

2-Acetylpyridine thiocarbonohydrazones : potent inactivators of herpes simplex virus ribonucleotide reductase

Pyrimido[4,5-c]pyridazines. 3. Preferential formation of 8-amino-1H-pyrimido[4,5-c]-1,2-diazepin-6(7H)-ones by cyclizations with .alpha.,.gamma.-dioxo esters

Pyrimido[4,5-c]pyridazines. 1. Cyclizations with .alpha.-keto esters

Pyrimido[4,5-c]pyridazines. VI: Pyrimido[4,5-c]pyridazines and 1,2,4-triazines from reactions between 6-hydrazinopyrimidin-4(3H)-ones and vicinal dicarbonyl reagents

Pyrimido[4,5-c]pyridazines. 2. Preferential formation of pyrimido[6,1-c][1,2,4]triazines by cyclizations with simple and complex .alpha.-halo ketones

Pyrimido[4,5-c]pyridazines. 5. Summary of cyclizations with vicinally functionalized reagents and studies of the reductive behavior of the ring system

1H-Pyrimido[4,5-c]-1,2-diazepines

Pyrimido[4,5-c]pyridazines. 4. Cyclizations with .alpha.-oxo acids

Substituted pyrimido (4,5-c)pyridazines

2,7-Diamino-8-methyl-5-substituted pyrido{2,3-d}pyrimidin-6-ones