A synthetic route to artificial chiral α-amino acids featuring a 3,4-dihydroisoquinolone core through a Rh(iii)-catalyzed functionalization of allyl groups in chiral Ni(ii) complexes

The first asymmetric synthetic route to artificial α-amino acids with a 3,4-dihydroisoquinolone skeleton was elaborated <jats:italic>via</jats:italic> a straightforward Rh(<jats:sc>iii</jats:sc>)-catalyzed C–H activation/annulation reaction.

Authors
Arsenov Mikhail A. 1 , Stoletova Nadezhda V. 1 , Smol'yakov Alexander F. 1, 2 , Savel'yeva Tat'yana F. 1 , Maleev Victor I. 1 , Loginov Dmitry A. 1, 2 , Larionov Vladimir A. 1, 3
Publisher
Royal Society of Chemistry
Issue number
46
Language
English
Pages
9143-9149
State
Published
Volume
21
Year
2023
Organizations
  • 1 A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences (INEOS RAS), Vavilov Str. 28, bld. 1, 119334 Moscow, Russian Federation
  • 2 Plekhanov Russian University of Economics, Stremyanny Per. 36, 117997 Moscow, Russian Federation
  • 3 Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya Str. 6, 117198 Moscow, Russian Federation
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