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

David M. Hodgson; Magnus W.P. Bebbington; Paul Willis

doi:10.1021/ol027039o

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

David M. Hodgson, Magnus W.P. Bebbington, Paul Willis

Chemistry and Biochemistry

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

23 Scopus citations

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 language	English
Pages (from-to)	4353-4356
Number of pages	4
Journal	Organic Letters
Volume	4
Issue number	24
DOIs	https://doi.org/10.1021/ol027039o
State	Published - 28 Nov 2002

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@article{fadd9979f501476d8578cd46e53a68a5,

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.",

author = "Hodgson, \{David M.\} and Bebbington, \{Magnus W.P.\} and Paul Willis",

year = "2002",

month = nov,

day = "28",

doi = "10.1021/ol027039o",

language = "English",

volume = "4",

pages = "4353--4356",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "24",

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

AU - Hodgson, David M.

AU - Bebbington, Magnus W.P.

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.

UR - https://www.scopus.com/pages/publications/0041736499

U2 - 10.1021/ol027039o

DO - 10.1021/ol027039o

M3 - Article

C2 - 12443096

AN - SCOPUS:0041736499

SN - 1523-7060

VL - 4

SP - 4353

EP - 4356

JO - Organic Letters

JF - Organic Letters

IS - 24

ER -

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

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