Asymmetric aldol reactions in ketone/ketone systems catalyzed by ionic liquid-supported C2-symmetrical organocatalyst

Asymmetric aldol reactions in ketone/ketone systems catalyzed by ionic liquid-supported C2-symmetrical organocatalyst Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2015, Volume: 25, Number: 3, Pages: 168-170 Pages count : 3 DOI: 10.1016/j.mencom.2015.05.002

Authors

Kochetkov Sergei V. ¹ , Kucherenko Alexander S. ¹ , Zlotin Sergei G. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Ionic liquid-supported (1S,2S)- and (1R,2R)-1,2-bis[(S)-prolinamido]-1,2-diphenylethanes act as organocatalysts in asymmetric aldol reactions of acetone with α-keto esters or trifluoroacetophenone providing high yields and from moderate to high enantioselectivity. Recycling of the catalyst with a gradual decrease in conversion and ee values is possible.

Kochetkov S.V. , Kucherenko A.S. , Zlotin S.G.
Asymmetric aldol reactions in ketone/ketone systems catalyzed by ionic liquid-supported C2-symmetrical organocatalyst
Mendeleev Communications. 2015. V.25. N3. P.168-170. DOI: 10.1016/j.mencom.2015.05.002 WOS Scopus OpenAlex

Web of science:	WOS:000357142000002
Scopus:	2-s2.0-84930948086
OpenAlex:	W973471862

DB	Citing
OpenAlex	19
Scopus	23
Web of science	24