The rearrangement of aromatic nitro-compounds in strongly acidic media

Peter Barrow; John V. Bullen; Andrea Dent; Timothy Murphy; John H. Ridd; Omaima Sabek

doi:10.1039/C39860001649

The rearrangement of aromatic nitro-compounds in strongly acidic media

Peter Barrow, John V. Bullen, Andrea Dent, Timothy Murphy, John H. Ridd, Omaima Sabek

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

10 Scopus citations

Abstract

2-Nitro-m-xylene and a number of nitrophenols undergo a 1,3-nitro-group rearrangement in trifluoromethanesulphonic acid at 70-110°C.

Original language	English (US)
Pages (from-to)	1649-1650
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	22
DOIs	https://doi.org/10.1039/C39860001649
State	Published - 1986

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Molecular Medicine

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Abdominal Transplant

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10.1039/C39860001649

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@article{bb62a492dc684fe983941ee26b2a855d,

title = "The rearrangement of aromatic nitro-compounds in strongly acidic media",

abstract = "2-Nitro-m-xylene and a number of nitrophenols undergo a 1,3-nitro-group rearrangement in trifluoromethanesulphonic acid at 70-110°C.",

author = "Peter Barrow and Bullen, \{John V.\} and Andrea Dent and Timothy Murphy and Ridd, \{John H.\} and Omaima Sabek",

note = "Funding Information: The authors would like to thank the National Science Council of Taiwan for financial support under the grant NSC-90-2212-E-005-009. Copyright: Copyright 2015 Elsevier B.V., All rights reserved.",

year = "1986",

doi = "10.1039/C39860001649",

language = "English (US)",

pages = "1649--1650",

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

issn = "0022-4936",

publisher = "Chemical Society",

number = "22",

}

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T1 - The rearrangement of aromatic nitro-compounds in strongly acidic media

AU - Barrow, Peter

AU - Bullen, John V.

AU - Dent, Andrea

AU - Murphy, Timothy

AU - Ridd, John H.

AU - Sabek, Omaima

N1 - Funding Information: The authors would like to thank the National Science Council of Taiwan for financial support under the grant NSC-90-2212-E-005-009. Copyright: Copyright 2015 Elsevier B.V., All rights reserved.

PY - 1986

Y1 - 1986

N2 - 2-Nitro-m-xylene and a number of nitrophenols undergo a 1,3-nitro-group rearrangement in trifluoromethanesulphonic acid at 70-110°C.

AB - 2-Nitro-m-xylene and a number of nitrophenols undergo a 1,3-nitro-group rearrangement in trifluoromethanesulphonic acid at 70-110°C.

UR - https://www.scopus.com/pages/publications/37049066671

UR - https://www.scopus.com/inward/citedby.url?scp=37049066671&partnerID=8YFLogxK

U2 - 10.1039/C39860001649

DO - 10.1039/C39860001649

M3 - Article

AN - SCOPUS:37049066671

SN - 0022-4936

SP - 1649

EP - 1650

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 22

ER -

The rearrangement of aromatic nitro-compounds in strongly acidic media

Abstract

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