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Direct synthesis of anilines and nitrosobenzenes from phenols
A one-pot synthesis of anilines and nitrosobenzenes from phenols has been developed using an ipso -oxidative aromatic substitution ( i S O Ar) process. The products are obtained in good yields under mild and metal-free conditions. The leaving group effect on reactions that proceed through mixed quio...
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Published in: | Organic & biomolecular chemistry 2016-01, Vol.14 (24), p.552-5524 |
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Language: | English |
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container_end_page | 5524 |
container_issue | 24 |
container_start_page | 552 |
container_title | Organic & biomolecular chemistry |
container_volume | 14 |
creator | St. Amant, A. H Frazier, C. P Newmeyer, B Fruehauf, K. R Read de Alaniz, J |
description | A one-pot synthesis of anilines and nitrosobenzenes from phenols has been developed using an
ipso
-oxidative aromatic substitution (
i
S
O
Ar) process. The products are obtained in good yields under mild and metal-free conditions. The leaving group effect on reactions that proceed through mixed quionone monoketals has also been investigated and a predictive model has been established.
A one-pot synthesis of anilines and nitrosobenzenes from phenols has been developed using an
ipso
-oxidative aromatic substitution (
i
S
O
Ar) process. |
doi_str_mv | 10.1039/c6ob00073h |
format | article |
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ipso
-oxidative aromatic substitution (
i
S
O
Ar) process. The products are obtained in good yields under mild and metal-free conditions. The leaving group effect on reactions that proceed through mixed quionone monoketals has also been investigated and a predictive model has been established.
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i
S
O
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ipso
-oxidative aromatic substitution (
i
S
O
Ar) process. The products are obtained in good yields under mild and metal-free conditions. The leaving group effect on reactions that proceed through mixed quionone monoketals has also been investigated and a predictive model has been established.
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ipso
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i
S
O
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ipso
-oxidative aromatic substitution (
i
S
O
Ar) process. The products are obtained in good yields under mild and metal-free conditions. The leaving group effect on reactions that proceed through mixed quionone monoketals has also been investigated and a predictive model has been established.
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ipso
-oxidative aromatic substitution (
i
S
O
Ar) process.</abstract><cop>England</cop><pmid>26848022</pmid><doi>10.1039/c6ob00073h</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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source | Royal Society of Chemistry |
title | Direct synthesis of anilines and nitrosobenzenes from phenols |
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