Bioinspired Total Synthesis of Bussealin E.
Organic Letters
(2018)
20
1597
(doi: 10.1021/acs.orglett.8b00340)
Loving the poison: the methylcitrate cycle and bacterial pathogenesis.
Microbiology (Reading)
(2018)
164
251
(doi: 10.1099/mic.0.000604)
Second-generation CK2α inhibitors targeting the αD pocket.
Chemical science
(2018)
9
3041
(doi: 10.1039/c7sc05122k)
Stapled peptides as a new technology to investigate protein-protein interactions in human platelets.
Chemical Science
(2018)
9
4638
(doi: 10.1039/x0xx00000x)
Diversity-oriented synthesis for the generation of N-substituted quaternary carbon containing small molecules from α,α-disubstituted propargyl amino esters
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2018)
256
Adventures in Drugging Undruggable Targets
JOURNAL OF PEPTIDE SCIENCE
(2018)
24
S44
The Application of Diversity-oriented Synthesis in Chemical Biology
(2018)
10
8
Highly Reactive Bis-Cyclooctyne-Modified Diarylethene for SPAAC-mediated Cross-Linking
Organic and Biomolecular Chemistry
(2018)
16
8559
(doi: 10.1039/C8OB02428F)
Using Peptidomimetics and Constrained Peptides as Valuable Tools for Inhibiting Protein-Protein Interactions
Molecules
(2018)
23
E959
(doi: 10.3390/molecules23040959)
Synthesis of diverse semi-saturated bicyclic heteroaromatics
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2018)
256
Site-selective generation of stable antibody-drug conjugates via cysteine bridging of native antibodies
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2018)
256
Stereocontrolled Semisyntheses of Elliptone and 12aβ-Hydroxyelliptone
Journal of Natural Products
(2017)
80
2751
(doi: 10.1021/acs.jnatprod.7b00527)
Structural and Functional Characterization of Malate Synthase G from Opportunistic Pathogen Pseudomonas aeruginosa.
Biochemistry
(2017)
56
5539
(doi: 10.1021/acs.biochem.7b00852)
Targeting the Genome‐Stability Hub Ctf4 by Stapled‐Peptide Design
Angewandte Chemie
(2017)
129
13046
(doi: 10.1002/ange.201705611)
Identification of new quorum sensing autoinducer binding partners in
Chemical science
(2017)
8
7403
(doi: 10.1039/c7sc01270e)
Targeting the Genome‐Stability Hub Ctf4 by Stapled‐Peptide Design
Angewandte Chemie International Edition
(2017)
56
12866
(doi: 10.1002/anie.201705611)
Computationally-guided optimization of small-molecule inhibitors of the Aurora A kinase-TPX2 protein-protein interaction.
Chemical communications (Cambridge, England)
(2017)
53
9372
(doi: 10.1039/c7cc05379g)
A fragment-based approach leading to the discovery of a novel binding site and the selective CK2 inhibitor CAM4066
Bioorganic & Medicinal Chemistry
(2017)
25
3471
(doi: 10.1016/j.bmc.2017.04.037)
An expedient strategy for the diversity-oriented synthesis of macrocyclic compounds with natural product-like characteristics
Tetrahedron
(2017)
72
3567
(doi: 10.1016/j.tet.2015.10.061)
Diversity-oriented synthesis of heterocycles and macrocycles by controlled reactions of oxetanes with α-iminocarbenes
Chemical science
(2017)
8
5713
(doi: 10.1039/c7sc00964j)