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

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

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2017, Volume: 66, Number: 2, Pages: 293-296 Pages count : 4 DOI: 10.1007/s11172-017-1730-y

Authors

Banina O.A. ¹ , Sudarikov D.V. ¹ , Nigmatov A.G. ² , Frolova L.L. ¹ , Slepukhin P.A. ³ , Zlotin S.G. ² , Kutchin A.V. ¹

Affiliations

1	Institute of Chemistry, Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences, Syktyvkar, Russian Federation
2	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
3	I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation

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.

Banina O.A. , Sudarikov D.V. , Nigmatov A.G. , Frolova L.L. , Slepukhin P.A. , Zlotin S.G. , Kutchin A.V.
Carane amino alcohols as organocatalysts in asymmetric aldol reaction of isatin with acetone
Russian Chemical Bulletin. 2017. V.66. N2. P.293-296. DOI: 10.1007/s11172-017-1730-y WOS Scopus OpenAlex

Web of science:	WOS:000405088100012
Scopus:	2-s2.0-85021789227
OpenAlex:	W2726940771

DB	Citing
OpenAlex	11
Scopus	14
Web of science	11