Alihough preview stu&s have shown that acyclic j3.r\_unsaturated oximea and oxime ethers do not undergo the aza-dl-mmethane {ADPM) rmrrangewmt. the Z-nu~l~,4dipAm~-2-~nylb~-3-~1 oxiww Sm. its wwhyl ether 51 and the 2,2.4,4-tetraphenylbnt-3-enal oxime I4 give the correapondhg cydopropyl derbatives &,
✦ LIBER ✦
The photochemical synthesis of potential pyrethroid components by the aza-di-π-methane rearrangement of β,γ-unsaturated oxime acetates.
✍ Scribed by Diego Armesto; Mar G. Gallego; William M. Horspool
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 245 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The synhses and phcbchmical mactbns of oxime m of ethyl 4,4dlmethyl+ oxopent-2+noate and ethyl 2,4,4-trimsthyl+oxo-2-enoate are described. The former compound undergoes E-Z_ oftheC=CbondwhllethelaUertearrangesbytheazadl+methans reactlontoafforda cydopropene derlvatlve.
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