## Abstract For Abstract see ChemInform Abstract in Full Text.
A new regioselective synthesis and bioactivity of 1H-pyrazolo[3,4-d]pyrimidin-4(5H)-one derivatives
✍ Scribed by Hong-Qing Wang; Zhao-Jie Liu; Li-Min Yang; Ming-Wu Ding
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2004
- Tongue
- English
- Weight
- 154 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
A series of new 1__H__‐pyrazolo[3,4‐d]pyrimidin‐4(5H)‐one Derivatives 5 has been designed and regio‐selectively synthesized via a tandem aza‐Wittig reaction. The structures of all compounds prepared have been confirmed by ^1^H NMR, IR, EI‐MS spectroscopy and elemental analyses. The results of preliminary bioassay indicate that most compounds 5 possess an inhibition effect against Botrytis cinereapers and Pyricularia oryzae at the concentration of 50 mg/L.
📜 SIMILAR VOLUMES
## Abstract magnified image A novel approach to regioselective synthesis of new 5‐amino‐6‐arylamino‐1__H__‐pyrazolo[3,4‐__d__]pyrimidin‐4(5__H__)‐one **5** derivatives __via__ a tandem aza‐wittig and annulation reaction of iminophosphorance **2**, aromatic isocyanates and hydrazine in 69.6–94.7% i
## Abstract A series of novel 1‐phenylthieno[1,2,4]triazolo[4,3‐__a__]pyrimidin‐5(4__H__)‐one derivatives **5** and **6** were synthesized by oxidative cyclization of thienopyrimidinonyl hydrazones using iodobenzene diacetate. J. Heterocyclic Chem., (2011).
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