## 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 of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
ChemInform Abstract: Haloheterocyclization of 2-Methallyl(propargyl)thioquinoline-3-carbaldehydes.
โ Scribed by M. Yu. Onysko; V. G. Lendel
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 26 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0931-7597
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๐ SIMILAR VOLUMES
## Abstract The synthesis of title compounds (II) involves a silverโcatalyzed 6โendoโdig acetalizationโcyclization followed by immediate hydrolysis of the unstable intermediates (III).
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
Acylation of Sterically Hindered 2-Propargyl-1,3-diketones. -The acylation of sterically hindered propargyl-substituted 1,3-diketones (I) by acyl chlorides occurs selectively at the terminal acetylenic group in the presence of CuCl. Some peculiarities of this reaction are reported. -(SHERGINA, S. I.