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
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.
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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. |
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