about
Cascade Oxidation/Halogenoaminocyclization Reaction of Trifluoromethylated Homoallylic N-Acylhydrazines: Metal-free Synthesis of CF3-Substituted Pyrazolines.Synthesis of trifluoromethylated pyrazolidines by [3 + 2] cycloaddition.Efficient synthesis of aliphatic sulfones by Mg mediated coupling reactions of sulfonyl chlorides and aliphatic halides.Phenyliodonium diacetate mediated carbotrifluoromethylation of N-acylhydrazones.Trichloroisocyanuric Acid Promoted Cascade Cyclization/Trifluoromethylation of Allylic Oximes: Synthesis of Trifluoromethylated Isoxazolines.Synthesis of Trifluoroethyl Pyrazolines via Trichloroisocyanuric Acid Promoted Cascade Cyclization/Trifluoromethylation of β,γ-Unsaturated HydrazonesVisible-light-promoted acyl radical cascade reaction for accessing acylated isoquinoline-1,3(2H,4H)-dione derivatives[3 + 2] Cycloaddition of para-Quinone Methides with Nitrile Imines: Approach to Spiro-pyrazoline-cyclohexadienonesSynthesis of Polysubstituted Trifluoromethylpyridines from Trifluoromethyl-α,β-ynonesTin Powder-Promoted Cascade Condensation/Allylation/Lactamization: Synthesis of Isoindolinones and Pyrazoloisoindol-8-onesVisible-light induced decarboxylative alkylation of quinoxalin-2(1H)-ones at the C3-positionElectrochemical Radical Formyloxylation-Bromination, -Chlorination, and -Trifluoromethylation of AlkenesDiastereoselective synthesis of spiro-cyclopropanyl-cyclohexadienones via direct sulfide-catalyzed [2 + 1] annulation of para-quinone methides with bromides
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Q47227398-A28EA0A3-9683-4265-9A25-C08BA7DDDD27Q47930306-3AF4D0F4-C1AC-4BB3-A6E9-5B369A5B9FBAQ48135884-5EE70D4C-34FC-4009-9C2F-785DAE07AF6EQ48234717-73B38B64-C3FD-4DFF-B6F3-FDB0665ABFD4Q51054871-E8BB8977-9A99-43F7-8C11-7B539748B287Q88224089-A703FFDA-1171-41BF-A2B9-F08C82F13825Q89891531-550D4C14-3D0A-4515-9D3A-80E7FC299235Q90297774-AC1E7885-AABC-4EB1-88B0-9C088C6E572BQ91950870-19BB5649-C01C-4100-8566-A32C30FFCECFQ92014180-BB4D2832-7073-43D4-A9B6-5E1A5CC3D310Q93011740-FE6FCC72-0E41-4566-973A-24B5CEB1C7A8Q93154945-855EA0A4-C8CC-4428-8098-99DDBE044204Q95645445-C1A698FC-3BA5-4E6D-8D79-92088C42E5A0
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description
researcher
@en
name
Yulai Hu
@en
type
label
Yulai Hu
@en
prefLabel
Yulai Hu
@en
P31
P496
0000-0002-9630-4150