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Chiral Amino‐Acid‐Amide Based Ionic Liquids as a Stereoselective Organocatalyst in Asymmetric Transfer Hydrogenation of Acetophenone at Room‐Temperature
Author(s) -
Javle Balasaheb R.,
Kinage Anil K.
Publication year - 2018
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201800240
Subject(s) - acetophenone , chemistry , transfer hydrogenation , amide , yield (engineering) , catalysis , ionic liquid , selectivity , stereoselectivity , asymmetric hydrogenation , noyori asymmetric hydrogenation , organic chemistry , enantioselective synthesis , materials science , ruthenium , metallurgy
Chiral Ionic Liquids (CILs) of amino acid amide were synthesized and used as novel organo catalyst for Asymmetric Transfer Hydrogenation (ATH) of acetophenone at room temperature. The developed CILs show very high yield and excellent enantio‐selectivity in transfer hydrogenation of acetophenone.