Corrigendum to “TMSCl-promoted selective oxidation of sulfides to sulfoxides with hydrogen peroxide” [Tetrahedron Lett. 51 (2010) 6939–6941]

Corrigendum to “TMSCl-promoted selective oxidation of sulfides to sulfoxides with hydrogen peroxide” [Tetrahedron Lett. 51 (2010) 6939–6941]

Tetrahedron Letters 52 (2011) 2002–2003 Contents lists available at ScienceDirect Tetrahedron Letters journal homepage: www.elsevier.com/locate/tetl...

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Tetrahedron Letters 52 (2011) 2002–2003

Contents lists available at ScienceDirect

Tetrahedron Letters journal homepage: www.elsevier.com/locate/tetlet

Corrigendum

Corrigendum to ‘‘TMSCl-promoted selective oxidation of sulfides to sulfoxides with hydrogen peroxide’’ [Tetrahedron Lett. 51 (2010) 6939–6941] Kiumars Bahrami a,⇑, Mohammad M. Khodaei a,⇑, Behrooz H. Yousefi b, Mehdi Sheikh Arabi a a b

Department of Chemistry, Razi University, Kermanshah 67149-67346, Iran Department of Nuclear Medicine, Klinikum rechts der Isar, Technische Universität München, Ismaninger Straße 22, D-81675 Munich, Germany

The authors regret that when this Letter was published the Sulfide and Sulfoxide entries for entry 4 were displayed incorrectly. The correct Table 2 is now reprinted below:

Table 2 Selective oxidation of sulfides to sulfoxides using the H2O2–TMSCl system in CH3CNa Entry

Sulfide

Sulfoxide

Yieldb (%)/time (min)

Mp (°C)

98 (2)

120–12216a

99 (20)

163–16416b

94 (15)

15816c

95 (2)

13216d

96 (3)

6816d

94 (10)

199–20116e

96 (10)

17215e

O S

S

1

O S

2

S

O2 N

O2 N

Br S

3

Me

Br

O S Me

O

4

S

S O

S

S

5

O

O

S

S

6c

O N 7

O

N S

N H

S N H

DOI of original article: 10.1016/j.tetlet.2010.10.171

⇑ Corresponding authors. Tel.: +98 831 4274559; fax: +98 831 4274559 (K.B.). E-mail addresses: [email protected] (K. Bahrami), [email protected] (M.M. Khodaei). 0040-4039/$ - see front matter Ó 2011 Elsevier Ltd. All rights reserved. doi:10.1016/j.tetlet.2011.02.072

2003

K. Bahrami et al. / Tetrahedron Letters 52 (2011) 2002–2003 Table 2 (continued) Entry

Sulfide

Mp (°C)

94 (3)

Oil16f

93 (35)

Oil16g

OH

98 (3)

151–15316h

CH3

98 (10)

39–4016d

92 (3)

29–3015c

95 (3)

Oil16i

O

S

S

8

O

O S

9

O

S

O

CH3

O

OH

S

O

S

CH3

S

10

11

Yieldb (%)/time (min)

Sulfoxide

O

CH3

S

H3C

H3C

S

O

12 13 a b c

S (CH3)2S

(CH3)2S@O 1

The purified products were characterized by mp and H and Yield refers to pure isolated product. 1,4-Dioxane was used as the solvent.

13

C NMR spectroscopy.