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THE MECHANISM OF ALKYL RADICAL LOSS FROM IONIZED PENTENYL METHYL AND HEXENYL METHYL ETHERS - THE IMPORTANCE OF A 1,2-HYDROGEN SHIFT TO THE RADICAL SITE OF A DISTONIC ION
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UNSPECIFIED (1992) THE MECHANISM OF ALKYL RADICAL LOSS FROM IONIZED PENTENYL METHYL AND HEXENYL METHYL ETHERS - THE IMPORTANCE OF A 1,2-HYDROGEN SHIFT TO THE RADICAL SITE OF A DISTONIC ION. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS (2). pp. 96-98. ISSN 0022-4936.
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Abstract
The crucial step in alkyl radical loss from various ionised pentenyl and hexenyl methyl ethers is shown by collision-induced dissociation experiments to involve a 1,2-H shift at the radical site of a distonic ion, followed by gamma-cleavage of the resultant ionised enol ether.
Item Type: | Journal Article | ||||
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Subjects: | Q Science > QD Chemistry | ||||
Journal or Publication Title: | JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | ||||
Publisher: | ROYAL SOC CHEMISTRY | ||||
ISSN: | 0022-4936 | ||||
Official Date: | 15 January 1992 | ||||
Dates: |
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Number: | 2 | ||||
Number of Pages: | 3 | ||||
Page Range: | pp. 96-98 | ||||
Publication Status: | Published |
Data sourced from Thomson Reuters' Web of Knowledge
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