Correction: Continuous flow photochemistry as an enabling synthetic technology: synthesis of substituted-6(5 H )-phenanthridinones for use as poly(ADP-ribose) polymerase inhibitors

Y. Fang; G. K. Tranmer

doi:10.1039/C6MD90011A

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DOI: 10.1039/C6MD90011A (Correction) Med. Chem. Commun., 2016, 7, 732-732

Correction: Continuous flow photochemistry as an enabling synthetic technology: synthesis of substituted-6(5H)-phenanthridinones for use as poly(ADP-ribose) polymerase inhibitors

Y. Fang ^a and G. K. Tranmer *^ab
^aCollege of Pharmacy, Faculty of Health Sciences, University of Manitoba, Winnipeg, MB R3E 0T5, Canada. E-mail: geoffrey.tranmer@umanitoba.ca
^bDepartment of Chemistry, Faculty of Science, University of Manitoba, Winnipeg, MB R3T 2N2, Canada

Received 23rd February 2016 , Accepted 23rd February 2016

First published on 29th February 2016

Abstract

Correction for ‘Continuous flow photochemistry as an enabling synthetic technology: synthesis of substituted-6(5H)-phenanthridinones for use as poly(ADP-ribose) polymerase inhibitors’ by Y. Fang et al., MedChemComm, 2016, DOI: 10.1039/c5md00552c.

The authors regret that Table 2 shows inconsistent entry numbering compared to Table 1. The corrected Table is shown below.

Table 2


Entry	R₁	R₂	R₃	R₄	R₅	R₆	Yield^a
a Isolated yields; 10 mL fluorinated ethylene propylene (FEP) coil, 60 °C, Vapourtech UV-150 medium pressure Hg lamp (75%, ∼112 W).
1	H	H	H	H	H	H	72
2	H	COMe	H	H	H	H	51
3	OMe	H	H	H	H	H	77
4	Cl	H	H	H	H	H	47
5	H	H	H	Cl	H	H	74

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

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