Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Jiang Tian Liu"'
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Akademický článek
Characterization of a recently synthesized microtubule-targeting compound that disrupts mitotic spindle poles in human cells
Autor: Dilan Boodhai Jaunky, Kevin Larocque, Mathieu C. Husser, Jiang Tian Liu, Pat Forgione, Alisa Piekny
Publikováno v: Scientific Reports, Vol 11, Iss 1, Pp 1-18 (2021)
Abstract We reveal the effects of a new microtubule-destabilizing compound in human cells. C75 has a core thienoisoquinoline scaffold with several functional groups amenable to modification. Previously we found that sub micromolar concentrations of C
Externí odkaz: https://doaj.org/article/761dc70f07fd464f93e17d7d415227ea
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6
Approaching the Integer‐Charge Transfer Regime in Molecularly Doped Oligothiophenes by Efficient Decarboxylative Cross‐Coupling
Autor: Jiang Tian Liu, Hannes Hase, Sarah Taylor, Ingo Salzmann, Pat Forgione
Publikováno v: Angewandte Chemie International Edition. 59:7146-7153
A library of symmetrical linear oligothiophene was prepared employing decarboxylative cross-coupling reaction as the key transformation. Thiophene potassium carboxylate salts were used as cross-coupling partners without the need of co-catalyst, base,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18661745786da2643e358baff487595c
https://doi.org/10.1002/anie.201914458
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7
Approaching the Integer‐Charge Transfer Regime in Molecularly Doped Oligothiophenes by Efficient Decarboxylative Cross‐Coupling
Autor: Hannes Hase, Sarah Taylor, Ingo Salzmann, Jiang Tian Liu, Pat Forgione
Publikováno v: Angewandte Chemie. 132:7212-7219
A library of symmetrical linear oligothiophene was prepared employing decarboxylative cross-coupling reaction as the key transformation. Thiophene potassium carboxylate salts were used as cross-coupling partners without the need of co-catalyst, base,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f06657f9df5248baf36edb9ecfca4f08
https://doi.org/10.1002/ange.201914458
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Design, structure-activity relationship study and biological evaluation of the thieno[3,2-c]isoquinoline scaffold as a potential anti-cancer agent
Autor: Mehdi Sirouspour, Alexandre Shafeii, Donald Campbell, Dilan B. Jaunky, Sarah Taylor, Keegan Mckibbon, Kevin Larocque, Helena Braga, Alisa Piekny, Fei Chen, Pat Forgione, Jiang Tian Liu
Publikováno v: Bioorganicmedicinal chemistry letters. 52
Several derivatives of a series that share a thienoisoquinoline scaffold have demonstrated potent activity against cancer cell lines A549, HeLa, HCT-116, and MDA-MB-231 in the submicromolar concentration range. Structure-activity relationship (SAR) s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0bcb73f60d2c007ccf9dbbc58c5d0e5
https://pubmed.ncbi.nlm.nih.gov/34416378
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9
A new reactive polymethacrylate bearing pendant furfuryl groups: Synthesis, thermoreversible reactions, and self-healing
Autor: Jiang Tian Liu, Sung Hwa Hong, Jung Kwon Oh, Dhamodaran Arunbabu, Sungmin Jung, Seung Man Noh
Publikováno v: Polymer. 109:58-65
We report a new methacrylate copolymer having pendant furfuryl groups (PFu) reactive to maleimide-bearing compounds to form thermally-induced crosslinked networks exhibiting self-healability through thermoreversible Diels-Alder (DA)/Retro-DA reaction
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5f484eaec7ef4081fe9284651ebe5307
https://doi.org/10.1016/j.polymer.2016.12.029
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10
Formation of Ion Pairs and Charge-Transfer Complexes in the p-Doping of Organic Semiconductors
Autor: Ingo Salzmann, Hannes Hase, Pat Forgione, Jiang Tian Liu
Publikováno v: ECS Meeting Abstracts. :760-760
The formation of ion pairs (IPA) through integer charge transfer and ground-state charge-transfer complexes (CPXs) with only fractional charge transfer are the two known mechanisms in the molecular doping of conjugated polymers and molecules, which f
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bf68c00300dc4689ad4cba0041d9485f
https://doi.org/10.1149/ma2020-018760mtgabs
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