A Facile Synthesis of Substituted 3,3,3-Trifluoropropenes by Oxidative Desulfurization-Fluorination of the Corresponding Dithiopropenoates. -Several substituted dithiopropenoates are directly converted to 3,3,3-trifluoropropenes by treatment with N-halosuccinimides according to A). The nitro-substi
ChemInform Abstract: 2-Bromo-3,3,3-trifluoropropene: A Facile Trifluoromethylacetylene Anion Synthon.
β Scribed by A. R. KATRITZKY; M. QI; A. P. WELLS
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
2-Bromo-3,3,3-trifluoropropene: A Facile Trifluoromethylacetylene Anion Synthon.
-Use of 2-bromo-3,3,3-trifluoropropene (I) provides a convenient and high yielding method to introduce a trifluoromethylethynyl moiety into a wide range of organic substrates (β (III); 8 examples).
π SIMILAR VOLUMES
## 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 βFull Textβ 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 βFull Textβ option. The original article is trackable v