✦ LIBER ✦

Studies on biologically active halogenated compounds. 1. Synthesis and central nervous system depressant activity of 2-(fluoromethyl)-3-aryl-4(3H)-quinazolinone derivatives

✍ Scribed by Tani, Junichi; Yamada, Yoshihisa; Oine, Toyonari; Ochiai, Takashi; Ishida, Ryuichi; Inoue, Ichizo

Book ID: 119949404
Publisher: American Chemical Society
Year: 1979
Tongue: English
Weight: 631 KB
Volume: 22
Category: Article
ISSN: 0022-2623
DOI: 10.1021/jm00187a021

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and evaluation of substituted

Synthesis and evaluation of substituted diphenyl-1,3,4-oxadiazole derivatives for central nervous system depressant activity

✍ Poonam Singh; Pramod Kumar Sharma; Jitendra Kumar Sharma; Anshu Upadhyay; Nitin 📂 Article 📅 2012 🏛 Springer-Verlag 🌐 English ⚖ 720 KB

Synthesis and Biological Activity of 6-E

Synthesis and Biological Activity of 6-Ethyl-4-aryl-5-methoxycarbonyl-3,4-dihydropyrimidin-2(1H)-ones.

✍ Selma Sarac; Murat Ciftci; Inci Selin Zorkun; Oezguel Tunc; Kevser Erol 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 20 KB 👁 1 views

Synthesis, structure and biological acti

Synthesis, structure and biological activity studies of 2-[(1H-1,2,4-triazol-1-yl)methyl]-1-aryl)-3-ferrocenyl prop-2-en-1-one derivatives

✍ Jianbing Liu; Tao Liu; Hong Dai; Zhong Jin; Jianxin Fang 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 127 KB 👁 1 views

ChemInform Abstract: Synthesis and Evalu

ChemInform Abstract: Synthesis and Evaluation of 2-Chloromethyl-3-N-substituted Arylthieno( 2,3-d)pyrimidin-4-ones and Derivatives for Central Nervous System Depressant Activity.

✍ K. S. MANJUNATH; S. MOHAN; L. V. G. NARAGUND; C. J. SHISHOO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

Convenient synthesis and biological acti

Convenient synthesis and biological activities of pyridine derivatives of 3,4-dihydropyrimidin-2(1H)-ones

✍ Xiao-Fei Zhu; De-Qing Shi 📂 Article 📅 2011 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 249 KB

## Abstract 2‐Chloro‐5‐(chloromethyl)‐pyridine reacted with 3,4‐dihydropyrimidin‐2(1H)‐ones **1** to afford 1‐[6‐aryl‐1‐(6‐chloropyridin‐3‐yl‐methyl)‐2‐(6‐chloropyridin‐3‐yl‐methylthio)‐4‐methyl‐1,6‐dihydropyrimidin‐5‐yl] carboxylates or ethanones **2** in good yields. The structure of the target c

1,3,4,6-tetracarbonyl systems. Part 8. S

1,3,4,6-tetracarbonyl systems. Part 8. Synthesis and antimicrobial activity of 2(5)-halogenated derivatives of 1,3,4,6-tetracarbonyl compounds

✍ E. N. Kozminykh; V. I. Goncharov; V. O. Kozminykh 📂 Article 📅 2008 🏛 Springer 🌐 English ⚖ 138 KB