Copper-catalyzed Csp2 –H amidation of unactivated arenes by N-tosyloxycarbamates

Alex John; Jeena Byun; Kenneth M. Nicholas

doi:10.1039/c3cc46412a

Copper-catalyzed Csp² –H amidation of unactivated arenes by N-tosyloxycarbamates

Alex John, Jeena Byun, Kenneth M. Nicholas

Chemistry (Twin Cities)

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

20 Scopus citations

Abstract

[(Neocuproine)Cu]PF₆ catalyzes the C–H amidation of unactivated arenes by N-tosyloxytrichloroethylcarbamates. Alkyl benzenes are selectively converted to aromatic amines and substituted arenes display variable regioselectivity.

Original language	English (US)
Pages (from-to)	10965-10967
Number of pages	3
Journal	Chemical Communications
Volume	49
Issue number	93
DOIs	https://doi.org/10.1039/c3cc46412a
State	Published - Oct 29 2013

Access

10.1039/c3cc46412a

Fingerprint Dive into the research topics of 'Copper-catalyzed Csp<sup>2</sup> –H amidation of unactivated arenes by N-tosyloxycarbamates'. Together they form a unique fingerprint.

Cite this

@article{046c706b558449feaa3ca77bc63b25c4,

title = "Copper-catalyzed Csp2 –H amidation of unactivated arenes by N-tosyloxycarbamates",

abstract = "[(Neocuproine)Cu]PF6 catalyzes the C–H amidation of unactivated arenes by N-tosyloxytrichloroethylcarbamates. Alkyl benzenes are selectively converted to aromatic amines and substituted arenes display variable regioselectivity.",

author = "Alex John and Jeena Byun and Nicholas, {Kenneth M.}",

year = "2013",

month = oct,

day = "29",

doi = "10.1039/c3cc46412a",

language = "English (US)",

volume = "49",

pages = "10965--10967",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "93",

}

TY - JOUR

T1 - Copper-catalyzed Csp2 –H amidation of unactivated arenes by N-tosyloxycarbamates

AU - John, Alex

AU - Byun, Jeena

AU - Nicholas, Kenneth M.

PY - 2013/10/29

Y1 - 2013/10/29

N2 - [(Neocuproine)Cu]PF6 catalyzes the C–H amidation of unactivated arenes by N-tosyloxytrichloroethylcarbamates. Alkyl benzenes are selectively converted to aromatic amines and substituted arenes display variable regioselectivity.

AB - [(Neocuproine)Cu]PF6 catalyzes the C–H amidation of unactivated arenes by N-tosyloxytrichloroethylcarbamates. Alkyl benzenes are selectively converted to aromatic amines and substituted arenes display variable regioselectivity.

UR - http://www.scopus.com/inward/record.url?scp=84886830614&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84886830614&partnerID=8YFLogxK

U2 - 10.1039/c3cc46412a

DO - 10.1039/c3cc46412a

M3 - Article

C2 - 24132225

AN - SCOPUS:84886830614

VL - 49

SP - 10965

EP - 10967

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 93

ER -