A novel synthesis of α,β-unsaturated nitriles from aromatic ketones via cyanophosphates
✍ Scribed by Shinya Harusawa; Ryuji Yoneda; Takushi Kurihara; Yasumasa Hamada; Takayuki Shioiri
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 134 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Reaction of aromatic ketones with diethyl phosphorocyanidate in the presence of lithium cyanide gave cyanophosphates, which were converted into a,@unsaturated nitriles by treatment with boron trifluoride etherate in high yields.
📜 SIMILAR VOLUMES
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
## Abstract A new approach to the synthesis of α, β‐unsaturated ketones from 1,2,3‐trimethyl benzimidazolium salt via the condensation reaction with aldehydes followed by the addition reaction of Grignard reagents with quaternary C=N bond was provided.