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Citation
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HERO ID
3686847
Reference Type
Journal Article
Title
Reductive rearrangement of 5-nitrobicyclo[2.2.1]hept-2-enes. Formation of 3-arylpyridines
Author(s)
Ho, TL; Liao, PY
Year
1994
Is Peer Reviewed?
1
Journal
Tetrahedron Letters
ISSN:
0040-4039
EISSN:
1873-3581
Publisher
Elsevier
Book Title
Tetrahedron Letters
Volume
35
Issue
14
Page Numbers
2211-2212
DOI
10.1016/S0040-4039(00)76799-2
Web of Science Id
WOS:A1994NE62100027
URL
https://linkinghub.elsevier.com/retrieve/pii/S0040403900767992
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Abstract
Abstract: Treatment of 6-aryl-5-nitrobicyclo[2.2.1]hept-2-enes with tin(II) chloride in refluxing THF or dioxane gave 3-arylpyridines via a deep-seated rearrangement. e field[29]: 1,4-Dioxane
Tags
OPPT REs
•
OPPT_1,4-Dioxane_D. Exposure
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