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Correction: Synthesis of indoles and quinazolines via additive-controlled selective C–H activation/annulation of N-arylamidines and sulfoxonium ylides
Ruizhi
Lai
,
Xiaohua
Wu
,
Songyang
Lv
,
Chen
Zhang
,
Maoyao
He
,
Yuncan
Chen
,
Qiantao
Wang
,
Li
Hai
* and
Yong
Wu
*
Key Laboratory of Drug-Targeting of Education Ministry and Department of Medicinal Chemistry, West China School of Pharmacy, Sichuan University, Chengdu 610041, China. E-mail: wyong@scu.edu.cn
First published on 6th August 2019
Abstract
Correction for ‘Synthesis of indoles and quinazolines via additive-controlled selective C–H activation/annulation of N-arylamidines and sulfoxonium ylides’ by Ruizhi Lai et al., Chem. Commun., 2019, 55, 4039–4042.
The authors regret that Table 2 was displayed incorrectly in the original article. The correct version is shown below.
| a Reaction conditions: N-arylethanimidamides 1 (0.20 mmol), dimethyloxosulfonium benzoylmethylide 2a (0.60 mmol), [Cp*RhCl2]2 (0.01 mmol), AgSbF6 (0.04 mmol), NaOAc (0.40 mmol) and DCE (1.0 ml) to a Schlenk tube. The mixture was stirred at 80 °C for 24 h under Ar. Then, without any post processing, the reaction mixture was purified by column chromatography on silica gel (eluent: PE/DCM = 1/1) to afford desired product. |
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The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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