Harald Jakobi
Overview
Explore the profile of Harald Jakobi including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
23
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0
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Recent Articles
1.
Alnafta N, Beffa R, Bojack G, Bollenbach-Wahl B, Brant N, Dornbrack C, et al.
J Agric Food Chem
. 2023 Jun;
71(47):18270-18284.
PMID: 37269295
There are several methods to control weeds, which impose particular challenges for farmers in all parts of the world, although applying small molecular compounds still remains the most efficient technology...
2.
Mattison R, Beffa R, Bojack G, Bollenbach-Wahl B, Dornbrack C, Dorn N, et al.
Pest Manag Sci
. 2023 Feb;
79(6):2264-2280.
PMID: 36815643
Background: Whilst there are several methods to control weeds, which continuously plague farmers around the globe, the application of small molecular compounds is still the most effective technology to date....
3.
Gierse R, Oerlemans R, Reddem E, Gawriljuk V, Alhayek A, Baitinger D, et al.
Sci Rep
. 2022 May;
12(1):7221.
PMID: 35508530
The development of drug resistance by Mycobacterium tuberculosis and other pathogenic bacteria emphasizes the need for new antibiotics. Unlike animals, most bacteria synthesize isoprenoid precursors through the MEP pathway. 1-Deoxy-D-xylulose...
4.
Gierse R, Reddem E, Alhayek A, Baitinger D, Hamid Z, Jakobi H, et al.
Biochem Biophys Res Commun
. 2021 Jan;
539:42-47.
PMID: 33421767
In this report, we describe a truncated Deinococcus radiodurans 1-deoxy-D-xylulose-5-phosphate synthase (DXS) protein that retains enzymatic activity, while slowing protein degradation and showing improved crystallization properties. With modern drug-design approaches...
5.
Synthesis of α-Chlorolactams by Cyanoborohydride-Mediated Radical Cyclization of Trichloroacetamides
Coussanes G, Jakobi H, Lindell S, Bonjoch J
Chemistry
. 2018 Apr;
24(32):8151-8156.
PMID: 29603478
A cyanoborohydride-promoted radical cyclization methodology has been developed to access α-chlorolactams in a simple and efficient way using NaBH CN and trichloroacetamides easily available from allylic and homoallylic secondary amines....
6.
Foster R, Adams H, Jakobi H, Harrity J
J Org Chem
. 2013 Apr;
78(8):4049-64.
PMID: 23548035
We report the synthesis and some structural studies of 4-trifluoromethyl, 4-difluoromethyl-, and 4-monofluoromethylsydnones. All but the latter compounds are stable and represent effective precursors to a range of pyrazoles after...
7.
Foster R, Jakobi H, Harrity J
Org Lett
. 2012 Sep;
14(18):4858-61.
PMID: 22934538
Two synthetic approaches to 4-trifluoromethylsydnones, a novel class of these mesoionic reagents, are reported. These compounds undergo regioselective alkyne cycloaddition reactions, thereby providing a general approach to 5-trifluoromethylpyrazoles. This method...
8.
De Matteis V, van Delft F, Jakobi H, Lindell S, Tiebes J, Rutjes F
J Org Chem
. 2006 Sep;
71(20):7527-32.
PMID: 16995655
A ring-closing metathesis mediated pathway to trifluoromethyl-containing piperidines is detailed. This involves the development of a synthetic route to a new (trifluoromethyl)allylating reagent via a Diels-Alder/retro-Diels-Alder strategy, its application in...