ThX-a next-generation probe for the early detection of amyloid aggregates
Chem Sci
(2020)
11
4578
(doi: 10.1039/c9sc04730a)
Functional Group Interaction Profiles: A General Treatment of Sol- vent Effects on Non-Covalent Interactions
Chemical Science
(2020)
11
4456
(doi: 10.1039/d0sc01288b)
Quantification of Cooperativity in the Self-Assembly of H-bonded Rosettes
Organic and Biomolecular Chemistry
(2020)
18
1602
(doi: 10.1039/d0ob00068j)
Two-component assembly of recognition-encoded oligomers that form stable H-bonded duplexes
Chemical Science
(2019)
11
561
(doi: 10.1039/c9sc04250d)
Molecular replication using covalent base-pairs with traceless linkers.
Org Biomol Chem
(2019)
17
9660
(doi: 10.1039/c9ob02336d)
A Synthetic Vesicle-to-Vesicle Communication System
Journal of the American Chemical Society
(2019)
141
17847
(doi: 10.1021/jacs.9b09102)
An Activatable Cancer-Targeted Hydrogen Peroxide Probe for Photoacoustic and Fluorescence Imaging.
Cancer research
(2019)
79
5407
Cap control: cyclic versus linear oligomerisation in covalent template-directed synthesis
RSC advances
(2019)
9
29566
(doi: 10.1039/c9ra07233k)
Molecular Transformer: A Model for Uncertainty-Calibrated Chemical Reaction Prediction
ACS Cent Sci
(2019)
5
1572
(doi: 10.1021/acscentsci.9b00576)
ThX – A next-generation probe for the early detection of amyloid aggregates
BIOPHYSICAL JOURNAL
(2019)
121
713594
(doi: 10.1101/713594)
Capping Strategies for Covalent Template-Directed Synthesis of Linear Oligomers Using CuAAC
J Am Chem Soc
(2019)
141
10862
(doi: 10.1021/jacs.9b04973)
Benchmarking of Halogen Bond Strength in Solution with Nickel Fluorides: Bromine versus Iodine and Perfluoroaryl versus Perfluoroalkyl Donors
Chemistry (Weinheim an der Bergstrasse, Germany)
(2019)
25
9237
(doi: 10.1002/chem.201900924)
Triaminopyrimidine derivatives as transmembrane HCl transporters
Organic & Biomolecular Chemistry
(2019)
17
5633
(doi: 10.1039/c9ob00725c)
Sequence information transfer using covalent template-directed synthesis
Chem Sci
(2019)
10
5258
(doi: 10.1039/c9sc01460h)
Emergent Supramolecular Assembly Properties of Recognition-Encoded Oligoesters
(2019)
(doi: 10.26434/chemrxiv.7795604)
Emergent Supramolecular Assembly Properties of a Recognition-Encoded Oligoester
Chemical Science
(2019)
10
5397
(doi: 10.1039/c9sc01669d)
Correction: Competitor analysis of functional group H-bond donor and acceptor properties using the Cambridge Structural Database.
Physical Chemistry Chemical Physics
(2019)
21
6296
(doi: 10.1039/c9cp90062d)
Building blocks for recognition-encoded oligoesters that form H-bonded duplexes.
Chem Sci
(2019)
10
2444
(doi: 10.1039/c8sc04896g)