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Correction: An asymmetric metal-templated route to amino acids with an isoquinolone core via a Rh(III)-catalyzed coupling of aryl hydroxamates with chiral propargylglycine Ni(II) complexes
Mikhail A.
Arsenov
a,
Nadezhda V.
Stoletova
a,
Tat'yana F.
Savel'yeva
a,
Alexander F.
Smol'yakov
ab,
Victor I.
Maleev
a,
Dmitry A.
Loginov
*ab and
Vladimir A.
Larionov
*ac
aA.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences (INEOS RAS), Vavilov Str. 28, 119991 Moscow, Russian Federation. E-mail: dloginov@ineos.ac.ru; larionov@ineos.ac.ru
bPlekhanov Russian University of Economics, Stremyanny Per. 36, 117997 Moscow, Russian Federation
cPeoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya Str. 6, 117198 Moscow, Russian Federation
First published on 28th March 2023
Abstract
Correction for ‘An asymmetric metal-templated route to amino acids with an isoquinolone core via a Rh(III)-catalyzed coupling of aryl hydroxamates with chiral propargylglycine Ni(II) complexes’ by Mikhail A. Arsenov et al., Org. Biomol. Chem., 2022, 20, 9385–9391, https://doi.org/10.1039/D2OB01970A.
The authors regret that there was an error in compound 1g shown in Scheme 2 (Ar = 3,5-F2Ph should read Ar = 2,3-F2Ph). The correct scheme is shown below. The structure has also been corrected in the updated ESI file.
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| Scheme 1 Substrate scope: evaluation of different Phe-derived Ni(II) complexes 1 with phenyl hydroxamate 2a. Combined isolated yields of the regioisomers 3 and 4 are shown in the parentheses. | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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