Synthesis of 6-Substituted-3-hydroxy-4(1H)-pyridinones: Oxidation-Michael Addition of 3-Hydroxy-4(1H)-pyridinones. -The oxidation of pyridinones of type (I) with Ag 2 O involving alcohols (II) is reported for the first time. The resulting pyridinediones subsequently undergo Michael addition with thi
Synthesis of substituted 1,2-benzoquinones and substituted 3-hydroxy-4 (1H)-pyridinones: Application of oxidation—Michael addition in organic synthesis
✍ Scribed by Miao-Sheng Li; Lin Ma; Xiao-Chun Zhang; Zhi-Shu Huang; Shao-Hua Xiao; Lian-Quan Gu
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 361 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0256-7660
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Pyridines 2-[ (Chloroacetyl)amino]acrylonitriles 1 and 3-[ (chloroacety1)-ridinones 8. Analogously to other orfho-diamines, the substi- (1.92 g, 20 mmol) and dry K2C03 (4.2 g, 30 mmol) in dioxane (15 ml) were stirred at 6 0 T , and chloroacetyl chloride (3.4 g, 30 mmol) was added dropwise with
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract magnified image Some new derivatives of spiro[3__H__‐indole‐3,2′‐thiazolidine]‐2,4′(1__H__)‐dione with the heterocyclic ring such as substituted thiazole and 1,2,4‐oxadiazole attached to the indolinone ring __via__ CH~2~ linkage has been synthesized in moderate yields. The synthesis ha