about
Practical Synthesis of Both Enantiomeric Amino Acid, Mannich, and Aldol Derivatives by Asymmetric Organocatalysis.Regulation of copper and iron homeostasis by metal chelators: a possible chemotherapy for Alzheimer's disease.Binding mechanism and synergetic effects of xanthone derivatives as noncompetitive α-glucosidase inhibitors: a theoretical and experimental study.Hypervalent Iodine Mediated Chemoselective Iodination of Alkynes.Development of Phenothiazine-Based Theranostic Compounds That Act Both as Inhibitors of β-Amyloid Aggregation and as Imaging Probes for Amyloid Plaques in Alzheimer's Disease.Synthesis of xanthone derivatives with extended pi-systems as alpha-glucosidase inhibitors: insight into the probable binding mode.Synthesis and pharmacological activities of xanthone derivatives as alpha-glucosidase inhibitors.Rationalization of the selectivity between 1,3- and 1,2-migration: a DFT study on gold(i)-catalyzed propargylic ester rearrangement.N4-Tetradentate chelators efficiently regulate copper homeostasis and prevent ROS production induced by copper-amyloid-β1-16, even in the presence of an excess of zinc.Frustrated Lewis Pair Catalyzed C-H Activation of Heteroarenes: A Stepwise Carbene Mechanism Due to Distance Effect.Chemoselective Preparation of 1-Iodoalkynes, 1,2-Diiodoalkenes, and 1,1,2-Triiodoalkenes Based on the Oxidative Iodination of Terminal AlkynesPhase-transfer-catalyzed asymmetric conjugate cyanation of alkylidenemalonates with KCN in the presence of a Brønsted acid additiveNonbifunctional Outer-Sphere Strategy Achieved Highly Active α-Alkylation of Ketones with Alcohols by N-Heterocyclic Carbene Manganese (NHC-Mn)Metal Ions in Alzheimer's Disease: A Key Role or Not?Mechanism of Hypervalent Iodine Promoted Fluorocyclization of Unsaturated Alcohols: Metathesis via Double Acids Activation
P50
Q39269116-A5647CD1-22EC-493B-8ABC-22F7987B3AD6Q40970249-20BAA8BB-BBE1-499E-AE3A-0ADA1B0372A0Q46680040-C7A44694-1758-4130-ACB7-466F4EBC136BQ47800037-4E81CAD9-3DCA-4245-9718-B33CF0D1B197Q48341612-AE7B289E-DB41-4086-A8B6-C2C6C39F48DDQ51057771-458A64B6-1EB1-43F9-BBDC-CECF5FF03A84Q51213252-A854AF3A-0AD5-46FC-B664-6A939AFF0EB6Q51444924-854FB14A-52D4-4386-994B-AE0160BE914CQ52691749-1BAD9A18-CF20-4CE0-9804-1069F5D29B95Q52699774-17C8A382-8F20-4925-87DD-AC6540BF9305Q57112700-40EF382A-14FD-45CF-8C21-62CE9A850864Q86277230-FED3B4BF-548B-4640-AB2F-0F1A621A8C5AQ90122903-E26C79F6-1DB2-4E72-B9DE-9F43800B5A56Q91630736-95ABC057-24AD-4D5B-B60E-19E778956E2FQ93382715-5C9D07F4-C3AD-402B-A7A8-6E5D2AB4CCCE
P50
description
researcher ORCID: 0000-0002-3864-1992
@en
name
Yan Liu
@ast
Yan Liu
@en
Yan Liu
@es
Yan Liu
@nl
Yan Liu
@sl
type
label
Yan Liu
@ast
Yan Liu
@en
Yan Liu
@es
Yan Liu
@nl
Yan Liu
@sl
prefLabel
Yan Liu
@ast
Yan Liu
@en
Yan Liu
@es
Yan Liu
@nl
Yan Liu
@sl
P1053
C-7832-2009
P106
P31
P3829
P496
0000-0002-3864-1992