L
Liu-Zhu Gong
Researcher at University of Science and Technology of China
Publications - 61
Citations - 3508
Liu-Zhu Gong is an academic researcher from University of Science and Technology of China. The author has contributed to research in topics: Enantioselective synthesis & Catalysis. The author has an hindex of 29, co-authored 61 publications receiving 3340 citations. Previous affiliations of Liu-Zhu Gong include Chinese Academy of Sciences & Nankai University.
Papers
More filters
Journal ArticleDOI
Design of organocatalysts for asymmetric direct syn-aldol reactions
TL;DR: Two new organocatalysts 3a and 3b, derived from L-leucine and (S)-beta-amino alcohols, were designed and afforded the direct syn-aldol reactions of a wide scope of aldehydes with various ketones with an excellent diastereomeric ratio of up to >20/1 and enantioselectivities ofup to 99% ee.
Journal ArticleDOI
Organocatalyzed highly enantioselective direct aldol reactions of aldehydes with hydroxyacetone and fluoroacetone in aqueous media: the use of water to control regioselectivity.
Xiao-Hua Chen,Shi-Wei Luo,Zhuo Tang,Linfeng Cun,Aiqiao Mi,Yaozhong Jiang,Liu-Zhu Gong,Liu-Zhu Gong +7 more
TL;DR: An organocatalyst prepared from (2R,3R)-diethyl 2-amino-3-hydroxysuccinate and L-proline exhibited high regio- and enantioselectivities for the direct aldol reactions of hydroxyacetone and fluoroacetone with aldehydes in aqueous media and it was found that water could be used to control the regioselectivity.
Journal ArticleDOI
The rational design of novel chiral oxovanadium(IV) complexes for highly enantioselective oxidative coupling of 2-naphthols.
TL;DR: Several chiral oxovanadium(IV) complexes have been designed and prepared for the asymmetric catalytic oxidative coupling of 2-naphthols with high enantioselectivities of 83-98% ee.
Journal ArticleDOI
Design of highly enantioselective organocatalysts based on molecular recognition.
TL;DR: A linear effect was observed for the reaction, demonstrating a single molecule of the catalyst involved in theCatalysis of ketones with aryl and alkyl alpha-keto acids.
Journal ArticleDOI
Asymmetric direct aldol reaction catalyzed by an L-prolinamide derivative: considerable improvement of the catalytic efficiency in the ionic liquid
TL;DR: The asymmetric direct aldol reactions of a wide scope of aldehydes with unmodified ketones in the presence of 20 mol%( S,S,S)-pyrrolidine-2-carboxylic acid and 2'-hydroxyl-1',2'-diphenyl-ethyl)-amine were performed.