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
Using peptidomimetics and constrained peptides as valuable tools for inhibiting protein-protein interactions
Molecules (Basel, Switzerland)
(2018)
23
959
(doi: 10.3390/molecules23040959)
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
Second-generation CK2α inhibitors targeting the αd pocket
Chem Sci
(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/c8sc00284c)
Adventures in Drugging Undruggable Targets
JOURNAL OF PEPTIDE SCIENCE
(2018)
24
S44
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 Pseudomonas aeruginosa using photoaffinity probes.
Chemical Science
(2017)
8
7403
(doi: 10.1039/c7sc01270e)
Targeting the Genome-Stability Hub Ctf4 by Stapled-Peptide Design.
Angew Chem Int Ed Engl
(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
(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 and 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)
Divergent synthesis of biflavonoids yields novel inhibitors of the aggregation of amyloid β (1-42)
Organic & Biomolecular Chemistry
(2017)
15
4554
(doi: 10.1039/c7ob00804j)
Stereocontrolled semi-syntheses of deguelin and tephrosin.
Organic & Biomolecular Chemistry
(2017)
15
1593
(doi: 10.1039/c6ob02659a)
(Z)-Selective Takai olefination of salicylaldehydes
Beilstein Journal of Organic Chemistry
(2017)
13
323
(doi: 10.3762/bjoc.13.35)