A number of 6-(4-phenoxyphenoxy)pyrimidines and triazines were synthesized and their herbicidal activity was measured. Compounds with the methoxy groups at the 2-and 4-positions on the pyrimidine and triazine rings exhibited high herbicidal activity. Introduction of a substituent into the 5position
Synthesis, enzyme — substrate interaction, and herbicidal activity of phosphoryl analogues of glycine
✍ Scribed by Natchev, Ivan A.
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 754 KB
- Volume
- 1988
- Category
- Article
- ISSN
- 0947-3440
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A new series of the 0-pyrimidinylsalicylates was synthesized and their herbicidal activity was examined. Some of these compounds showed very strong herbicidal activity under pre-and post-emergent treatment conditions against various kinds of grass and broadleaf weeds. Among these compounds, 0-(4, 6d
## Abstract A series of pyrimidinyl benzylamine analogues containing a phosphonyl group (**2**) was synthesized via the Mannich‐type reactions of 2‐(4,6‐dimethoxypyrimidin‐2‐yloxy)benzoaldehyde **1**, aromatic amines, and dialkyl phosphites or triphenyl phosphite in the presence of Mg(ClO~4~)~2~. T
## Abstract Aurora‐A is an oncogenic kinase that plays essential roles in mitosis as well as cell survival. Aurora‐A interacting protein (AIP) was identified as a negative regulator of Aurora‐A with its ectopic over expression inducing destabilization of Aurora‐A protein. Here we present evidence t