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IJMSInternational Journal of Molecular Sciences
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30 April 2014

Correction: Al-Majid, A.M., et al., Tandem Aldol-Michael Reactions in Aqueous Diethylamine Medium: A Greener and Efficient Approach to Bis-Pyrimidine Derivatives. Int. J. Mol. Sci. 2013, 14, 23762–23773.

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1
Department of Chemistry, Faculty of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
2
Department of Chemistry, Faculty of Science, Alexandria University, P.O. Box 426-Ibrahimia, Alexandria 21321, Egypt
3
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia
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Author to whom correspondence should be addressed.
Int. J. Mol. Sci.2014, 15(5), 7537-7538;https://doi.org/10.3390/ijms15057537
This article belongs to the Section Green Chemistry
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The authors wish to change Figure 2 in Section 2 of their paper published in IJMS [1]. Figure 2 is revised as follows. The authors and publisher apologize for any inconvenience.
Ijms 15 07537 g002 550
Figure 2. ORTEP representation of the structure of 3a–c.
Figure 2. ORTEP representation of the structure of 3a–c.
Ijms 15 07537 g002

Reference

  1. Al-Majid, A.M.; Barakat, A.; Al-Najjar, H.J.; Mabkhot, Y.N.; Ghabbour, H.A.; Fun, H.-K. Tandem Aldol-Michael reactions in aqueous diethylamine medium: A greener and efficient approach to bis-pyrimidine derivatives. Int. J. Mol. Sci 2013, 14, 23762–23773. [Google Scholar]

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