2-azabenzonorbornanes from 7-azabenzonorbornanols by a nitrogen-directed neophyl-type radical rearrangement

David M. Hodgson, Magnus Bebbington, Paul Willis

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

(equation presented) Barton deoxygenation of 7-azabenzonorbornanols leads to a synthetically useful neophyl-like rearrangement to give 2-azabenzonorbornane derivatives in 64-90% yields.

Original languageEnglish
Pages (from-to)4353-4356
Number of pages4
JournalOrganic Letters
Volume4
Issue number24
DOIs
StatePublished - 28 Nov 2002

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deoxygenation
Nitrogen
Derivatives
nitrogen

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title = "2-azabenzonorbornanes from 7-azabenzonorbornanols by a nitrogen-directed neophyl-type radical rearrangement",
abstract = "(equation presented) Barton deoxygenation of 7-azabenzonorbornanols leads to a synthetically useful neophyl-like rearrangement to give 2-azabenzonorbornane derivatives in 64-90{\%} yields.",
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2-azabenzonorbornanes from 7-azabenzonorbornanols by a nitrogen-directed neophyl-type radical rearrangement. / Hodgson, David M.; Bebbington, Magnus; Willis, Paul.

In: Organic Letters, Vol. 4, No. 24, 28.11.2002, p. 4353-4356.

Research output: Contribution to journalArticle

TY - JOUR

T1 - 2-azabenzonorbornanes from 7-azabenzonorbornanols by a nitrogen-directed neophyl-type radical rearrangement

AU - Hodgson, David M.

AU - Bebbington, Magnus

AU - Willis, Paul

PY - 2002/11/28

Y1 - 2002/11/28

N2 - (equation presented) Barton deoxygenation of 7-azabenzonorbornanols leads to a synthetically useful neophyl-like rearrangement to give 2-azabenzonorbornane derivatives in 64-90% yields.

AB - (equation presented) Barton deoxygenation of 7-azabenzonorbornanols leads to a synthetically useful neophyl-like rearrangement to give 2-azabenzonorbornane derivatives in 64-90% yields.

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