Erratum: Platinum nanoparticles supported on zirconia mediated synthesis of N-acyl and N-(tert-butoxycarbonyl)amines from nitroarenes and azides (Journal of Molecular Catalysis A: Chemical (2012) 355 (96-101) DOI: 10.1016/j.molcata. 2011.12.002)

Full text of DOI:10.1016/j.molcata.2012.01.016

Journal of Molecular Catalysis A: Chemical 357 (2012) 175–176
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Journal of Molecular Catalysis A: Chemical
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Erratum
Erratum to “Platinum nanoparticles supported on zirconia mediated synthesis
of N-acyl and N-(tert-butoxycarbonyl)amines from nitroarenes and azides”
[J. Mol. Catal. A: Chem. 355 (2012) 96–101]
a,∗
a
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M. Lakshmi Kantam , R. Sudarshan Reddy , K. Srinivas , R. Chakravarti ,
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B. Sreedhar , F. Figueras , Ch. Venkat Reddy
Inorganic and Physical Chemistry Division, Indian Institute of Chemical Technology, Hyderabad 500607, India
Institut de recherche sur la catalyse et l’environnement de Lyon, UMR 5256 Université Lyon 1-CNRS, 2, Avenue Albert Einstein, F-69626, Villeurbanne, France
311 Gilman Hall, Department of Chemistry, Iowa State University, Ames, IA 50011, USA
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1
The publisher regrets that when the above paper was published errors occurred in Table 4 and in Table 6.
The correct Table 4 is produced below.
In Table 6 Product was incorrectly spelt.
The publisher and authors would like to apologize for these errors.
Table 4
Reductive acylation of various nitroarenes catalysed by Pt(0)/ZrO2.a
Entry
ArNO2
Amide
Timeb
3
Timec
3.5
Yield%d
1
NO
2
NHAc
93,92,91,91e
2
3
4
5
6
7
8
I
NO
2
I
NHAc
3.5
3.5
3.5
3
4
87
92
91
92
92
88
87
Cl
NO
Cl
NHAc
4
2
Br
NO
Br
NHAc
NHAc
NHAc
5
2
F
NO
F
3.5
4.5
4.5
4.5
2
H3C
H3CO
OHC
NO
H3C
H3CO
OHC
4
2
NO
NHAc
4
2
NO
NHAc
4
2
DOI of original article: 10.1016/j.molcata.2011.12.002.
Corresponding author. Tel.: +91 40 27193510; fax: +91 40 27160921.
E-mail address: mlakshmi@iict.res.in (M.L. Kantam).
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381-1169/$ – see front matter © 2012 Elsevier B.V. All rights reserved.
doi:10.1016/j.molcata.2012.01.016

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M.L. Kantam et al. / Journal of Molecular Catalysis A: Chemical 357 (2012) 175–176
Table 4 (continued).
Entry
ArNO2
Amide
Timeb
4
Timec
4.5
Yield%d
89
9
HOOC
NO
2
HOOC
NHAc
10
11
12
HO
NO
2
HO
NHAc
3.5
4
4
5
5
93
75
68
H3COC
H3COOC
NO
H3COC
H3COOC
NHAc
2
NO
NHAc
4
2
a
b
c
Reaction conditions: nitroarene (1.0 mmol), Pt(0)/ZrO2 catalyst (0.15 mol%) methanol (4.0 mL), H2 balloon (1 atm), Ac2O (1.5 mmol), room temperature.
Time taken for first step (reduction of nitroarene to aminoarene).
Total reaction time.
Isolated yields after column chromatography.
Isolated yield in fourth cycle.
d
e