Erratum: Transition metal-free procedure for the synthesis of S-aryl dithiocarbamates using aryl diazonium fluoroborate in water at room temperature (Green Chemistry (2011) 13 (1837-1842) DOI: 10.1039/C1GC00001B))

Full text of DOI:10.1039/c1gc90050a

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ADDITIONS & CORRECTIONS
www.rsc.org/greenchem | Green Chemistry
Selective conversion of trioses to lactates over Lewis acid heterogeneous catalysts
Li Li, Christophe Stroobants, Kaifeng Lin, Pierre A. Jacobs, Bert F. Sels and Paolo P. Pescarmona
Green Chem., 2011, DOI: 10.1039/c0gc00923g.
A sentence was mistakenly omitted from the end of part 1 of the Experimental section. The final sentence of the part 1 should be:
Prior to the catalytic test, gallium oxide was reacted for 4 h at 80 ◦C with cyclooctene and aqueous H2O2 in ethyl acetate to remove
the Cl-species still present in the material, and then washed with ethanol and dried overnight at 90 ◦C.27
LCA approach to the analysis of solvent waste issues in the pharmaceutical industry
Michael J. Raymond, C. Stewart Slater and Mariano J. Savelski
Green Chem., 2010, 12, 1826–1834, (DOI: 10.1039/c003666h).
On page 1828, Table 1, the “THF” row and “Water kg” column value should read, 1.26E-01, instead of 2.31E-03.
All of the other values in the table are correct and this value is not used incorrectly anywhere else in the paper.
Production of liquid hydrocarbon fuels by catalytic conversion of biomass-derived levulinic acid
Drew J. Braden, Carlos A. Henao, Jacob Heltzel, Christos C. Maravelias and James A. Dumesic
Green Chem., 2011, DOI: 10.1039/c1gc15047b.
The fourth author’s name should read Christos T. Maravelias, instead of Christos C. Maravelias.
This journal is
The Royal Society of Chemistry 2011
Green Chem., 2011, 13, 3505–3508 | 3505
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Transition metal-free procedure for the synthesis of S-aryl dithiocarbamates using aryl diazonium fluoroborate in water at room
temperature
Tanmay Chatterjee, Sukalyan Bhadra and Brindaban C. Ranu
Green Chem., 2011, 13, 1837–1842 (DOI: 10.1039/C1GC00001B). Amendment published 2nd September 2011.
On page 1839, in Table 1 in entries 18–22, the figures under Yield and Time/h are interchanged. The correct representation of these
rows is provided below.
Table 1 Transition metal-free coupling of aryl diazonium tetrafluoroborate with dithiocarmate anions
Entry
18
R
Amine
Product
Yield (%)a
76
Time/h
3.5
Ref.
3-COCH3
19
20
4-I
4-I
84
91
3
2.8
21
22
4-I
83
92
3
3
4-CI
a Isolated yields of pure products (by 1H- and 13C-NMR).
3506 | Green Chem., 2011, 13, 3505–3508
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The Royal Society of Chemistry 2011
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Easy access to thiazolines and thiazines via tandem S-alkylation-cyclodeamination of thioamides/haloamines
Uma Pathak, Shubhankar Bhattacharyya, Vishwanath Dhruwansh, Lokesh Kumar Pandey, Rekha Tank and
Malladi V. S. Suryanarayana
Green Chem., 2011, 13, 1648–1651 (DOI: 10.1039/C1GC15285H). Amendment published 7th November 2011.
In Table 1 on page 1649, the product structures for entries 4, 5, 6, 7 and 9 are incorrect. The correct structures are provided below.
Table 1 Formation of thiazolines and thiazines from thioamides and haloamines
Entry no.
4.
Thioamide
Amine·HBr/HCl
Producta
Yield (%)b
83
Time
3 h
mp (◦C)
41–4217a
5.
6.
7.
9.
89
87
90
87
2 h
43–4417b
2.5 h
2.5 h
25 min
90–9217c
198–19917c
150–15217b
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
Additions and corrections can be viewed online by accessing the original article to which they apply.
This journal is
The Royal Society of Chemistry 2011
Green Chem., 2011, 13, 3505–3508 | 3507
©

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