Thioepoxide formation by ring closure of allylthiyl radicals - a novel rearrangement of allylic thionitrites.
2394 - 2395.
Tertiary allylic thionitrites undergo thermal rearrangement to alpha,beta-episulfide nitroso dimers via ring closure of allylthiyl radicals.
|Title:||Thioepoxide formation by ring closure of allylthiyl radicals - a novel rearrangement of allylic thionitrites|
|Keywords:||INDUCED EPOXIDE FRAGMENTATION, NITRIC-OXIDE, OXIRANYLCARBINYL RADICALS, INTRAMOLECULAR ADDITION, INDUCED DECOMPOSITION, ALPHA-IODOEPOXIDES, CONVENIENT METHOD, ATOM ABSTRACTION, ALKOXY RADICALS, ALKYL RADICALS|
|UCL classification:||UCL > School of BEAMS > Faculty of Maths and Physical Sciences
UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry
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