about
Stereocontrolled synthesis of (-)-galanthamineSynthesis and derivatisation of a novel spiro[1-benzofuran-2,4'-piperidin]-3-one scaffold.trans-2-Tritylcyclohexanol as a chiral auxiliary in permanganate-mediated oxidative cyclization of 2-methylenehept-5-enoates: application to the synthesis of trans-(+)-linalool oxide.Tetrazine-trans-cyclooctene ligation for the rapid construction of 18F labeled probes.Diastereoselective syntheses of (3R*,4R*)- and (3R*,4S*)-4-aryl-3-methyl-4-piperidinemethanol and fluoro analogues.C-H insertion approach to the synthesis of endo,exo-furofuranones: synthesis of (+/-)-asarinin, (+/-)-epimagnolin A, and (+/-)-fargesin.Permanganate oxidation of 1,5,9-trienes: stereoselective synthesis of tetrahydrofuran-containing fragments.Developments in furan syntheses.Synthesis of the non-adjacent bis-THF core of cis-sylvaticin using a double oxidative cyclisation.Total synthesis and stereochemical assignment of cis-uvariamicin I and cis-reticulatacin.Synthesis of isotopically labeled all-trans retinals for DNP-enhanced solid-state NMR studies of retinylidene proteins.A large geometric distortion in the first photointermediate of rhodopsin, determined by double-quantum solid-state NMR.Light penetration and photoisomerization in rhodopsin studied by numerical simulations and double-quantum solid-state NMR spectroscopy.Flow Electrolysis Cells for the Synthetic Organic Chemistry Laboratory.Electrochemical Deprotection of para-Methoxybenzyl Ethers in a Flow Electrolysis Cell.N-Heterocyclic Carbene-Mediated Microfluidic Oxidative Electrosynthesis of Amides from Aldehydes.N-Heterocyclic Carbene-Mediated Oxidative Electrosynthesis of Esters in a Microflow Cell.Long-lived localization in magnetic resonance imaging.Analytical theory of gamma-encoded double-quantum recoupling sequences in solid-state nuclear magnetic resonance.Substituent interference on supramolecular assembly in urea gelators: synthesis, structure prediction and NMR.A Resin-linker-vector approach to radiopharmaceuticals containing 18F: application in the synthesis of O-(2-[18F]-fluoroethyl)-L-tyrosine.Correction: Substituent interference on supramolecular assembly in urea gelators: synthesis, structure prediction and NMR.Double-quantum 13C nuclear magnetic resonance of bathorhodopsin, the first photointermediate in mammalian visionDetection of nerve agent via perturbation of supramolecular gel formationA biaryl cross-coupling strategy for functionalisation of benzocrown ethersEnhancement of quantum rotor NMR signals by frequency-selective pulsesReal-space imaging of macroscopic diffusion and slow flow by singlet tagging MRITheory of long-lived nuclear spin states in methyl groups and quantum-rotor induced polarisationLong-Lived Nuclear Spin States in Methyl Groups and Quantum-Rotor-Induced PolarizationSyntheses of 13C2-labelled 11Z-retinalsA Two-Directional Synthesis of (+)-β-IsosparteineTotal Synthesis of the Tetracyclic Lupin Alkaloid (+)-AllomatrineTotal Syntheses of (−) Epilupinine and (−)-Tashiromine Using Imino-Aldol ReactionsEnantioselective Formal Synthesis of Eurylene: Synthesis of thecis- andtrans-THF Fragments Using Oxidative CyclizationTotal synthesis of annonaceous acetogenins belonging to the non-adjacent bis-THF and non-adjacent THF-THP sub-classesNatural cis-solamin is a mixture of two tetra-epimeric diastereoisomers: biosynthetic implications for Annonaceous acetogeninsA metal–oxo mediated approach to the synthesis of 21,22-diepi-membrarollinIntramolecular C–H insertions adjacent to sulfur for the diastereoselective synthesis of thienofuranonesSynthesis of Heterocyclic and Carbocyclic Fluoro-olefins by Ring-Closing MetathesisSynthesis ofcis-Solamin Using a Permanganate-Mediated Oxidative Cyclization
P50
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P50
description
researcher ORCID ID = 0000-0003-0156-7087
@en
wetenschapper
@nl
name
Richard C.D. Brown
@ast
Richard C.D. Brown
@en
Richard C.D. Brown
@es
Richard C.D. Brown
@nl
type
label
Richard C.D. Brown
@ast
Richard C.D. Brown
@en
Richard C.D. Brown
@es
Richard C.D. Brown
@nl
prefLabel
Richard C.D. Brown
@ast
Richard C.D. Brown
@en
Richard C.D. Brown
@es
Richard C.D. Brown
@nl
P1153
55519858500
P31
P496
0000-0003-0156-7087