Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Julie Schmauck"'
Publikováno v:
Journal of Functional Biomaterials, Vol 9, Iss 1, p 21 (2018)
In this study, the efficacy of electron beam irradiation versus chemical coupling for yielding polyethersulfone (PES) membranes with antibacterial properties was investigated. For the surface coating, a recently discovered lead compound, IL-KKA, comp
Externí odkaz:
https://doaj.org/article/6f2ede6b1a624e38a41966ac28348e41
Autor:
Michael S. Perryman, Julian Riegger, Julie Schmauck, Bertrand Schweitzer-Chaput, Martin Breugst, Huilan Yue, Rik H. Verschueren, Martin Klussmann
Publikováno v:
Chemistry – A European Journal. 25:9088-9097
In this work, the reactivities of acetonyl and benzoyl radicals in aromatic substitution and addition reactions have been compared in an experimental and computational study. The results show that acetonyl is more electrophilic than benzoyl, which is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f4564ba8ceaf3d97073e23fdb940e73
https://doi.org/10.1002/chem.201901439
https://doi.org/10.1002/chem.201901439
Autor:
Marcus Brauns, Martin Breugst, Jörg Pietruszka, Patrick Ullrich, Julie Schmauck, Marvin Mantel
Publikováno v:
The journal of organic chemistry 85(4), 1894-1905 (2020). doi:10.1021/acs.joc.9b02573
Herein we show a novel approach toward the allylation of indoles. Thereby, we explore a class of bench-stable allylboronates and fine-tune their reactivity. The allylations of different substituted indoles proceed with negligible diastereo- and excel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9266e2131a2c8c287b17698bbb7d9505
https://hdl.handle.net/2128/26891
https://hdl.handle.net/2128/26891
Autor:
Julie Schmauck, Martin Breugst
Publikováno v:
Nachrichten aus der Chemie. 66:862-865
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1e313478a90f29e6862baa39117b325
https://doi.org/10.1002/nadc.20184077309
https://doi.org/10.1002/nadc.20184077309
Publikováno v:
Synthesis. 49:3224-3236
Noncovalent interactions play an important role in many biological and chemical processes. Among these, hydrogen bonding is very well studied and is already routinely used in organocatalysis. This Short Review focuses on three other types of promisin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1756cc548f6d8de448c1908c3c3e220
https://doi.org/10.1055/s-0036-1588838
https://doi.org/10.1055/s-0036-1588838
Publikováno v:
Journal of Functional Biomaterials
Journal of Functional Biomaterials, Vol 9, Iss 1, p 21 (2018)
Journal of Functional Biomaterials; Volume 9; Issue 1; Pages: 21
Journal of Functional Biomaterials, Vol 9, Iss 1, p 21 (2018)
Journal of Functional Biomaterials; Volume 9; Issue 1; Pages: 21
In this study, the efficacy of electron beam irradiation versus chemical coupling for yielding polyethersulfone (PES) membranes with antibacterial properties was investigated. For the surface coating, a recently discovered lead compound, IL-KKA, comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::810838b6bd4274709907d7a358710db1
http://europepmc.org/articles/PMC5872107
http://europepmc.org/articles/PMC5872107
Autor:
Julie Schmauck, Martin Breugst
Publikováno v:
Organicbiomolecular chemistry. 15(38)
Pnicogen bonding is a noncovalent interaction between the electrophilic region of a phosphorus atom and a Lewis base. Although this interaction can be comparable in strength to other noncovalent interactions, no systematic application in organic synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a60172433cc27e91c6c950dc3070949b
https://pubmed.ncbi.nlm.nih.gov/28770945
https://pubmed.ncbi.nlm.nih.gov/28770945
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 23(50)
An optimized protecting group for allylboronates allowed the use of ketones in order to synthesize all isomers of quaternary homoallylic alcohols with high enantioselectivities. All symmetric isomers of the allylboronate were prepared in high yields
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6be9d085b27d77e498171003896e7160
https://pubmed.ncbi.nlm.nih.gov/28423201
https://pubmed.ncbi.nlm.nih.gov/28423201