Correction: An overview of the applications of chiral phosphoric acid organocatalysts in enantioselective additions to C=O and C=N bonds

Abstract

Correction for ‘An overview of the applications of chiral phosphoric acid organocatalysts in enantioselective additions to C=O and C=N bonds’ by Xabier del Corte et al., Org. Chem. Front., 2022, 9, 6331–6399, https://doi.org/10.1039/D2QO01209J.

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The authors regret that there were some minor errors in Tables 1 and 2 in the original article. The correct versions of Tables 1 and 2 are provided herein.

Table 1 Summary of BINOL-derived chiral phosphoric acid organocatalysts. (R enantiomer shown)

Cat.	R^1	R^2	Cat.	R^1	R^2
BPA1	H	9-Phenanthryl	BPA23	H	3,5-Ph2C6H3
BPA2	H	2,4,6-(^iPr)3C6H2	BPA24	H	^tBu
BPA3	H	2,4,6-(Cy)3C6H2	BPA25	H	4-PhC6H4
BPA4	H	2,4,6-(Me)3C6H2	BPA26	H	CPh2OH
BPA5	H	3,5-(CF3)2C6H3	BPA27	H	3,5-(2,4,6-(CH3)3C6H2)2C6H3
BPA6	H	I	BPA28	H	1-Naphthyl
BPA7	H	C6F5	BPA29	PPh3^+PF6^−	2,4,6-(^iPr)3C6H2
BPA8	H	2-Naphthyl	BPA30	H	2,6-(^iPr)2-4-(9-anthryl)-C6H2
BPA9	H	Ph	BPA31	H	4-Adamantyl-2,6-(^iPr)2C6H2
BPA10	H	SiPh3	BPA32	H	4-^tBu-C6H4
BPA11	H	2,4,6-(Me)3-3,5-(NO2)2C6	BPA33	H	P(4-CH3C6H4)^+ B(3,5-(CF3)2C6H3)4^−
BPA12	H	Cy	BPA34	H	C6(CH3)5
BPA13	H	3,5-(^tBu)2-4-OMeC6H2	BPA35	C8H17
BPA14	H	3,5-(4-FC6H4)2C6H3
BPA15	H	9-Anthryl
BPA16	H	4-^tBu-2,6-(Me)2C6H2	BPA36	H		R: ^iPr
BPA17	H	Si(4-^tBuC6H4)3	BPA37	H		R: 1-naphthyl
BPA18	H	Me	BPA38	H		R: Et
BPA19	H	4-NO2C6H4	BPA39	H		R: tolyl
BPA20	H	4-(2-Naphthyl)-C6H4
BPA21	H	4-ClC6H4
BPA22	I	2,4,6-(^iPr)3C6H2

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Table 2 Summary of chiral phosphoric acid organocatalysts. (R enantiomer shown)

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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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