AbstractÐA convenient synthesis of a-diones and their monoprotected acetals, i.e. a-ketoacetals, was developed by mercury induced solvolysis of regiospeci®cally formed a-chloro-a-(alkylthio)ketones. Analogously, a-alkoxy-a-sulfenylated ketones were formed when reacting a-chloro-a-sulfenylated ketone
Regiospecific preparation of α,α-dihalofluoromethyl perfluoroalkyl ketones
✍ Scribed by In Howa Jeong; Donald J. Burton; Daryl G. Cox
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 201 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Acylation of E-phosphoranium salts with E-acyl chlorides gives the corresponding Z-perfluoro betaine in high yield.
Subsequent chlorination or bromination regiospecifically yields the a,d-dihalofluoromethyl perfluoroalkyl ketones.
📜 SIMILAR VOLUMES
lsomeric en01 ester, enamine, and silyl enol ether derivatives of unsymmetrical ketones are converted regiospecifically to d-arylsulfonoxy ketones with arylsulfonyl peroxides.
C CH 2 Ar Cl CF 3 (CF 2 ) n •, O 2 Perfluoroalkylated Heterocyclic Compounds NuH, Na 2 CO 3 3: Nu= OMe ether C CH 2 Ph Cl 1) CF 3 (CF 2 ) 5 I, (Bu 3 Sn) 2 , hν, O 2 , benzene 2) Et 3 N, Na 2 CO 3 , ether C C
## 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 “Full Text” option. The original article is trackable v