Formation of 1-aza-allyl radicals from 2-halogenoalkylamines

Iain MacInnes; John C. Walton

doi:10.1039/C39860001604

Formation of 1-aza-allyl radicals from 2-halogenoalkylamines

Iain MacInnes, John C. Walton^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

Abstract

Hydrogen abstraction from 2-halogenoethylamines is followed by dehydrohalogenation to give 1-aza-allyl radicals which show significantly greater spin density at the CH₂ terminus than do allyl radicals.

Original language	English
Pages (from-to)	1604-1605
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	21
DOIs	https://doi.org/10.1039/C39860001604
Publication status	Published - 1 Jan 1986

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title = "Formation of 1-aza-allyl radicals from 2-halogenoalkylamines",

abstract = "Hydrogen abstraction from 2-halogenoethylamines is followed by dehydrohalogenation to give 1-aza-allyl radicals which show significantly greater spin density at the CH2 terminus than do allyl radicals.",

author = "Iain MacInnes and Walton, \{John C.\}",

year = "1986",

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doi = "10.1039/C39860001604",

language = "English",

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journal = "Journal of the Chemical Society, Chemical Communications",

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AU - MacInnes, Iain

AU - Walton, John C.

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N2 - Hydrogen abstraction from 2-halogenoethylamines is followed by dehydrohalogenation to give 1-aza-allyl radicals which show significantly greater spin density at the CH2 terminus than do allyl radicals.

AB - Hydrogen abstraction from 2-halogenoethylamines is followed by dehydrohalogenation to give 1-aza-allyl radicals which show significantly greater spin density at the CH2 terminus than do allyl radicals.

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M3 - Article

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JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 21

ER -

Formation of 1-aza-allyl radicals from 2-halogenoalkylamines

Abstract

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