about
Highly enantioselective and efficient organocatalytic aldol reaction of acetone and β,γ-unsaturated α-keto ester.C-Aryl glucoside SGLT2 inhibitors containing a biphenyl motif as potential anti-diabetic agents.Chiral phosphoric acid catalyzed highly enantioselective Friedel-Crafts alkylation reaction of C3-substituted indoles to β,γ-unsaturated α-ketimino esters.Catalytic and highly enantioselective Friedel-Crafts alkylation of aromatic ethers with trifluoropyruvate under solvent-free conditionsOrganocatalytic asymmetric domino aza-Michael-Mannich reaction: synthesis of tetrahydroimidazopyrimidine derivativesRegio and Enantioselective Organocatalytic Friedel-Crafts Alkylation of 4-Aminoindoles at the C7-PositionOne-Pot Enantioselective Synthesis of 2-Pyrrolidinone Derivatives Bearing a Trifluoromethylated All-Carbon Quaternary StereocenterChiral Phosphoric-Acid-Catalyzed Regioselective and Enantioselective C7-Friedel-Crafts Alkylation of 4-Aminoindoles with Trifluoromethyl Ketones
P50
Q42821957-CCD98129-E646-4B93-9E78-82FE59438533Q51626836-D06687EA-B52A-48B7-B5B1-A4C4BBFDECA5Q51666373-7EB5F1CF-A7CD-47CD-AD9C-9EA5550A4DCAQ79430344-0A58796E-D92E-47E5-A5EC-4CEE86209621Q84737410-47524EA1-6120-4AAA-A9E2-10921F20C6DFQ89887788-2B03AE06-30D3-4304-8826-67B2DC446F19Q91350110-57FDDCD6-9DBE-4DC8-B567-3E24B5B7A7ADQ91781614-6304F4A2-122B-43AE-867C-D25A005AFAF2
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Junling Zhao
@ast
Junling Zhao
@en
Junling Zhao
@es
Junling Zhao
@nl
Junling Zhao
@sl
type
label
Junling Zhao
@ast
Junling Zhao
@en
Junling Zhao
@es
Junling Zhao
@nl
Junling Zhao
@sl
prefLabel
Junling Zhao
@ast
Junling Zhao
@en
Junling Zhao
@es
Junling Zhao
@nl
Junling Zhao
@sl
P106
P1153
16247000400
P31
P496
0000-0002-2960-0830