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 via a straightforward Rh(iii)-catalyzed C–H activation/annulation reaction.
Авторы
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
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
Hakobyan Hegine I., Jamgaryan Silva M., Sargsyan Armen S., Danghyan Yuri M., Larionov Vladimir A., Maleev Victor I., Saghyan Ashot S., Mardiyan Zorayr Z.