Carane amino alcohols as organocatalysts in asymmetric aldol reaction of isatin with acetone


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Resumo

Carane-derived β-amino alcohols with amino and hydroxy groups at positions 3 and 4 differing in their mutual arrangement and configuration were synthesized. Their application as organocatalysts in the asymmetric aldol reaction of isatin with acetone allowed one to obtain adducts with up to 84% enantiomeric excess.

Sobre autores

O. Banina

Institute of Chemistry, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

Autor responsável pela correspondência
Email: olga.ferolg.banina@mail.ru
Rússia, 48 ul. Pervomaiskaya, Syktyvkar, 167000

D. Sudarikov

Institute of Chemistry, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

Email: olga.ferolg.banina@mail.ru
Rússia, 48 ul. Pervomaiskaya, Syktyvkar, 167000

A. Nigmatov

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: olga.ferolg.banina@mail.ru
Rússia, 47 Leninsky prosp., Moscow, 119991

L. Frolova

Institute of Chemistry, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

Email: olga.ferolg.banina@mail.ru
Rússia, 48 ul. Pervomaiskaya, Syktyvkar, 167000

P. Slepukhin

I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences

Email: olga.ferolg.banina@mail.ru
Rússia, 22 ul. S. Kovalevskoi, Ekaterinburg, 620219

S. Zlotin

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: olga.ferolg.banina@mail.ru
Rússia, 47 Leninsky prosp., Moscow, 119991

A. Kutchin

Institute of Chemistry, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences

Email: olga.ferolg.banina@mail.ru
Rússia, 48 ul. Pervomaiskaya, Syktyvkar, 167000

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