✦ LIBER ✦

Synthetic uses of the sequential ring positional reactivity in Pyridin-3-ol and derivatives

✍ Scribed by Clark, GJ; Deady, LW

Book ID: 117995010
Publisher: Commonwealth Scientific and Industrial Research Organisation Publishing
Year: 1981
Tongue: English
Weight: 244 KB
Volume: 34
Category: Article
ISSN: 0004-9425
DOI: 10.1071/ch9810927

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Cyclic 1,3-Diones and Their Derivatives

Cyclic 1,3-Diones and Their Derivatives as Versatile Reactive Intermediates in the Syntheses of Condensed Fused Ring Heterocycles

✍ Batchu Chandra Sekhar 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 8 KB 👁 2 views

Flavan-3-ol derivatives are positive mod

Flavan-3-ol derivatives are positive modulators of GABAA receptors with higher efficacy for the α2 subtype and anxiolytic action in mice

✍ Sebastian P. Fernandez; Kenneth N. Mewett; Jane R. Hanrahan; Mary Chebib; Graham 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 627 KB

Nitropyrazoles. 11. Isomeric 1-methyl-3(

Nitropyrazoles. 11. Isomeric 1-methyl-3(5)-nitropyrazole-4-carbonitriles in nucleophilic substitution reactions. Comparative reactivity of the nitro group in positions 3 and 5 of the pyrazole ring

✍ I. L. Dalinger; A. A. Zaitsev; T. K. Shkineva; S. A. Shevelev 📂 Article 📅 2004 🏛 Springer 🌐 English ⚖ 288 KB

Nitropyrazoles. Part 11. Isomeric 1-Meth

Nitropyrazoles. Part 11. Isomeric 1-Methyl-3(5)-nitropyrazole-4-carbonitriles in Nucleophilic Substitution Reactions. Comparative Reactivity of the Nitro Group in Positions 3 and 5 of the Pyrazole Ring.

✍ I. L. Dalinger; A. A. Zaitsev; T. K. Shkineva; S. A. Shevelev 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 150 KB 👁 1 views

Investigation the chemical reactivity of

Investigation the chemical reactivity of positions N-3, C-5 and C6-methyl group in biginelli type compounds and synthesis of new dihydropyrimidine derivatives

✍ Y. R. Mirzaei; H. Azamat; H. Namazi 📂 Article 📅 2001 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 45 KB 👁 1 views

## Abstract The compounds 5‐ethoxycarbonyl‐1,6‐dimethyl‐4‐(3‐nitrophenyl)‐3,4‐dihydropyrimidin‐2(l__H__)‐one (5) and 5‐ethoxycarbonyl‐1‐phenyl‐6‐methyl‐4‐(3‐nitrophenyl)‐3,4‐dihydropyrimidin‐2(l__H__)‐one (1) were prepared by the Biginelli condensation method and they converted to eight N‐3 substit

Electrophilic substitution in benzo[b]th

Electrophilic substitution in benzo[b]thieno- and benzo[b]furo[2,3-c]pyridines. Use of the nuclear overhauser effect for determination of substitution position

✍ S. V. Tolkunov; M. N. Kal'nitskii; V. I. Dulenko 📂 Article 📅 1997 🏛 Springer US 🌐 English ⚖ 173 KB