Open Access Article
This Open Access Article is licensed under a
Creative Commons Attribution 3.0 Unported Licence

Correction: Metal-free tandem reaction synthesis of spiro-cyclopropyl fused pyrazolin-5-one derivatives

Man Liu a, Chen-Fei Liu a, Jing Zhang a, Yan-Jun Xu *b and Lin Dong *a
aKey Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, West China School of Pharmacy, Sichuan University, Chengdu 610041, China. E-mail: dongl@scu.edu.cn
bCollege of Chemistry and Material Science, Sichuan Normal University, Chengdu, Sichuan 610066, China. E-mail: xuyj@sicnu.edu.cn

Received 28th February 2019 , Accepted 28th February 2019

First published on 14th March 2019


Abstract

Correction for ‘Metal-free tandem reaction synthesis of spiro-cyclopropyl fused pyrazolin-5-one derivatives’ by Man Liu et al., Org. Chem. Front., 2019, 6, 664–668.


The authors regret that in Fig. 1, Table 2 and Scheme 3 previous versions of the graphics were inadvertently included above the correct graphics. The correct versions are shown below.
image file: c9qo90021g-f1.tif
Fig. 1 Bioactive spiro-pyrazolone heterocyclic molecules.
Table 2 Substrate scope of N-arylpyrazol-5-onesa
a Unless otherwise mentioned all reactions were performed with 0.05 mmol of 1, 3.0 equiv. of 2a, 3.0 equiv. of p-nitrobenzoic acid, toluene (0.5 mL), 120 °C, 12 h, under air. Isolated yield.
image file: c9qo90021g-u1.tif



image file: c9qo90021g-s3.tif
Scheme 3 Proposed reaction mechanism.

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


This journal is © the Partner Organisations 2019
Click here to see how this site uses Cookies. View our privacy policy here.