about
Seamless integration of dose-response screening and flow chemistry: efficient generation of structure-activity relationship data of β-secretase (BACE1) inhibitors.A convenient photocatalytic fluorination of unactivated C-H bonds.Prospective Evaluation of Free Energy Calculations for the Prioritization of Cathepsin L Inhibitors.18F-Fluorination of Unactivated C-H Bonds in Branched Aliphatic Amino Acids: Direct Synthesis of Oncological Positron Emission Tomography Imaging Agents.CHEMICAL SYNTHESIS. Going with the flow.A Convenient Late-Stage Fluorination of Pyridylic C-H Bonds with N-Fluorobenzenesulfonimide.Inverse Electron-Demand [4 + 2]-Cycloadditions of Ynamides: Access to Novel Pyridine Scaffolds2 H-1,2,3-Triazole-Based Dipeptidyl Nitriles: Potent, Selective, and Trypanocidal Rhodesain Inhibitors by Structure-Based DesignDirect heterobenzylic fluorination, difluorination and trifluoromethylthiolation with dibenzenesulfonamide derivatives.Determination of End-to-End Distances in a Series of TEMPO Diradicals of up to 2.8 nm Length with a New Four-Pulse Double Electron Electron Resonance ExperimentLinear Monodisperse π-Conjugated Oligomers: Model Compounds for Polymers and MoreMonodisperse Poly(triacetylene) Rods: Synthesis of a 11.9 nm Long Molecular Wire and Direct Determination of the Effective Conjugation Length by UV/Vis and Raman SpectroscopiesSynthesis of annulated pyridines as inhibitors of aldosterone synthase (CYP11B2)Quaternary Ammonium Trifluoromethoxide Salts as Stable Sources of Nucleophilic OCF3Paracrine crosstalk between intestinal L- and D-cells controls secretion of glucagon-like peptide-1 in miceA Convenient Synthesis of Difluoroalkyl Ethers from Thionoesters Using Silver(I) FluorideSite-Selective, Late-Stage C-H 18 F-Fluorination on Unprotected Peptides for Positron Emission Tomography ImagingSynthesis of acyl fluorides via photocatalytic fluorination of aldehydic C-H bonds18F-Branched-Chain Amino Acids: Structure-Activity Relationships and PET Imaging PotentialModulation of Pharmacologically Relevant Properties of Piperidine Derivatives by Functional Groups in an Equatorial or Axial β-Position to the Amino Group
P50
Q30741444-A260734B-C8E4-4D55-89E9-DF3B1E73EE88Q34412063-8CCD81D4-363C-4D74-B51D-9DE999AC06A2Q48045269-0D5BF48B-B89F-4714-B99D-0BB307EC623BQ48179727-943A6D49-A034-429A-ABCD-D52C495FDE51Q53920769-4967ADF8-48D3-49B1-BD5B-F09D5272DF1AQ54611862-5DE30708-FFAC-4949-9CB4-7EAF5D2D3A54Q57776740-7327C52D-8D2A-4FB3-9DF8-7257EC23ACE6Q58842290-2254383A-C411-4DF5-BFF6-0F19F14FFA0AQ64924481-AB058A0F-9111-4F02-A895-B5E3282FCACAQ88519535-E8D1BB86-D0A6-4E4B-8203-23EE345EF2E7Q88520937-1F25C642-29F8-4B08-BF5B-D5F62FA49002Q88521512-335B260B-65DB-4148-B520-E8B8DBB10D70Q89335674-DAC0F119-0D33-4233-8A1B-AAF93EA3CCBEQ89694808-8CB5D0FA-4EED-45B3-871E-A7082697478AQ90020443-DD066349-2029-4B66-B32A-F9C7E9122D66Q90185743-D18062C5-BD08-4459-ABBD-8A3BC28818B8Q90817001-B69F0961-6EB4-4A18-925E-DDE8024EDFF3Q91032857-CD3F9017-2FB2-4343-8CBF-8F33F1C7582FQ91228923-CDD2EDA8-A3BA-42B0-9C0D-D4DCD258F70DQ93147984-9A7AC782-D081-4E30-8B76-C76926072006
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Rainer E Martin
@en
Rainer E Martin
@nl
type
label
Rainer E Martin
@en
Rainer E Martin
@nl
prefLabel
Rainer E Martin
@en
Rainer E Martin
@nl
P31
P496
0000-0001-7895-497X