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Correction: Bifunctional organic sponge photocatalyst for efficient cross-dehydrogenative coupling of tertiary amines to ketones

Teng Zhang , Weiwei Liang , Yuxing Huang , Xingrong Li , Yizhen Liu , Bo Yang , Chuanxin He , Xuechang Zhou and Junmin Zhang *
College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, 518060, P. R. China. E-mail: zhangjm@szu.edu.cn

Received 15th August 2018 , Accepted 15th August 2018

First published on 28th August 2018


Abstract

Correction for 'Bifunctional organic sponge photocatalyst for efficient cross-dehydrogenative coupling of tertiary amines to ketones' by Teng Zhang et al., Chem. Commun., 2017, 53, 12536–12539.


The authors regret that there was an error in Table 1 in the original article. The figures in brackets were missing in the final entry in the “yield” column of the table. The correct version of Table 1 is presented below.
Table 1 Optimization of reaction conditionsa

image file: c8cc90374c-u1.tif

Entry x Solvent Yieldb (%)
a Reactions were performed using 1a (0.1 mmol) and 2a (1.0 mmol) in 2 mL of solvent and were catalyzed by sponge catalyst A-7 at room temperature with a 12 W green LED light for 24 hours. b Yield was determined by 1H NMR with 1,3,5-trimethoxybenzene as an internal standard. c <2% ee, determined by chiral HPLC analysis on an AS-H column. d Isolated yield; 7.4% ee. e The yield in the absence of LED irradiation. f The yield in the dark.
1 2 THF Trace
2 2 Toluene Trace
3 2 DCM Trace
4 2 EA 9
5 2 Dioxane 6
6 2 EtOH 15
7 2 NMP Trace
8 2 DMF 18
9 2 ACN 12
10 2 DMSO Trace
11 2 2-Methyl-2-pentanol 30c
12 2 H 2 O 81
13 1.5 H2O 72
14 3 H 2 O 95 (93 , 36 , 11 )


The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.


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