about
The complexity of catalysis: origins of enantio- and diastereocontrol in sulfur ylide mediated epoxidation reactions.Effect of sulfide structure on enantioselectivity in catalytic asymmetric epoxidation of aldehydes: mechanistic insights and implications.Unraveling the mechanism of epoxide formation from sulfur ylides and aldehydes.A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationaTotal synthesis of citrafungin A.Reactivity and selectivity in the Wittig reaction: a computational study.Kinetic Resolution of 2-Substituted Indolines by N-Sulfonylation using an Atropisomeric 4-DMAP-N-oxide Organocatalyst.A Method for Identifying and Developing Functional Group Tolerant Catalytic Reactions: Application to the Buchwald-Hartwig Amination.On the origin of high E selectivity in the Wittig reaction of stabilized ylides: importance of dipole-dipole interactions.Cyclometalated Iridium-PhanePhos Complexes Are Active Catalysts in Enantioselective Allene-Fluoral Reductive Coupling and Related Alcohol-Mediated Carbonyl Additions That Form Acyclic Quaternary Carbon StereocentersTotal synthesis of aigialomycin D using a one-pot ketene generation-trapping-aromatization sequenceTwo-step cyanomethylation protocol: convenient access to functionalized aryl- and heteroarylacetonitrilesShort, Gram-Scale Syntheses of β- and γ-Lycorane Using Two Distinct Photochemical ApproachesImproved Substrate Scope in the Potassium Hexacyanoferrate(II)-Based Cyanation for the Synthesis of Benzonitriles and Their Heterocyclic AnaloguesSynthesis and Pharmacological Characterization of 2-(2,6-Dichlorophenyl)-1-((1S,3R)-5-(3-hydroxy-3-methylbutyl)-3-(hydroxymethyl)-1-methyl-3,4-dihydroisoquinolin-2(1H)-yl)ethan-1-one (LY3154207), a Potent, Subtype Selective, and Orally Available PosRhodium-Catalyzed Aldehyde Arylation via Formate-Mediated Transfer Hydrogenation: Beyond Metallic Reductants in Grignard/Nozaki-Hiyami-Kishi-Type Addition
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Q35597919-79BFD561-CAF2-46C8-BE71-8F4E7E7D0A6CQ37681676-46A6E11C-D041-42C1-9F8F-FC698E4A43E0Q40640514-B03F3702-6A7D-413D-A76F-CA21B1791D53Q44571465-12DDF383-CB28-439D-AE52-15D98B4BED48Q46332968-018BA269-9295-4679-B141-5CD74782DA3BQ46944362-1033CC40-BDE6-43E4-91EF-67A63D2125AAQ47566197-7A4F9379-8476-45D6-AD60-38D2B7715FCBQ47566546-443B1F27-2826-4539-9AA3-B8FE6E8408ECQ47605393-84E22535-FC5F-406D-8347-4445BAC6FA9CQ64174733-EE701DB9-4BE9-424D-80EF-0EBC0D14E988Q84620344-81C9F180-CE3E-4FD1-A850-75DDFAA2E6A7Q86534674-1730AB9C-DDC7-4A22-8DBC-E198ED994FB6Q87795090-67197DCA-EC73-43CF-B02A-92073612B5D6Q88307707-B74ADC2B-5F0E-437E-BCC7-C6A5C4388C6BQ90160447-D5D655C3-5C52-4751-819A-9FBC0CDCC202Q91263000-0E4B5A48-767D-455E-AB9C-0F27EFE9C578
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jeffery Richardson
@ast
Jeffery Richardson
@en
Jeffery Richardson
@es
Jeffery Richardson
@nl
type
label
Jeffery Richardson
@ast
Jeffery Richardson
@en
Jeffery Richardson
@es
Jeffery Richardson
@nl
prefLabel
Jeffery Richardson
@ast
Jeffery Richardson
@en
Jeffery Richardson
@es
Jeffery Richardson
@nl
P106
P31
P496
0000-0002-4450-3828