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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

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✦ 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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The aza-di-π-methane rearrangement of β-
✍ Diego Armesto; Ana Ramos; Elena P. Mayoral 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 343 KB

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 &,