Results 51 to 60 of about 35,784 (226)

Generative and Experimental Validation of High Refractive Index Polymers via Domain Knowledge Approach with Small Data

open access: yesAdvanced Intelligent Discovery, EarlyView.
This research demonstrates that the combination of domain knowledge–based multiple regression, multi‐objective Bayesian optimization, and generative models is a suitable prediction tool for candidates of high refractive index polymers, even with the constraints in the model trained on limited data. The experimental validation can reproduce the proposed
Takuya Yokoo   +3 more
wiley   +1 more source

Synthesis of 2,3-dihydronaphtho[2,3-d][1,3]thiazole-4,9-diones and 2,3-dihydroanthra[2,3-d][1,3]thiazole-4,11-diones and novel ring contraction and fusion reaction of 3H-spiro[1,3-thiazole-2,1'-cyclohexanes] into 2,3,4,5-tetrahydro-1H-carbazole-6,11-diones

open access: yesBeilstein Journal of Organic Chemistry, 2013
Treatment of N-substituted 2-(methylamino)naphthoquinones 3 and -anthracene-1,4-diones 4 with S2Cl2 and DABCO in chlorobenzene gave the corresponding 2,3-dihydronaphtho[2,3-d][1,3]thiazole-4,9-diones 1 and 2,3-dihydroanthra[2,3-d][1,3]thiazole-4,11 ...
Lidia S. Konstantinova   +3 more
doaj   +1 more source

Synthesis and biological evaluation of thiazole and metergoline derivatives as antimycobacterial and antiplasmodial agents [PDF]

open access: yes, 2013
TB patients show poor compliance to available drugs due to the costs, adverse side effects, and prolonged treatment, leading to multi-drug resistant (MDR), extensively drug resistant (XDR), and most recently totally drug resistant TB.
Mjambili, Faith Riziki
core   +1 more source

Effect of Thiazole Derivatives on Copper Corrosion in Acidic Sulphate Solution

open access: yesInternational Journal of Electrochemical Science, 2015
Inhibition of copper corrosion in 0.1 mol dm-3 Na2SO4 solution (pH 3) by two thiazole derivatives of 5-(5'-methylfurfurylidene-2')-2,4-dioxotetrahydro-1,3-thiazole (MFDT) and 2-thiono-5-(4'-ethoxybenzylidene)-4-oxotetrahydro-1,3-thiazole (TEBOT) was ...
Jelena Nakomčić   +3 more
doaj   +1 more source

Overview on Biological Activities of Thiazole Derivatives [PDF]

open access: yesRecords of Pharmaceutical & Biomedical Sciences
Thiazole and its derivatives have garnered widespread attention in medicinal chemistry due to their remarkable range of biological activities. This heterocyclic scaffold is characterized by a five-membered aromatic ring that incorporates both nitrogen ...
Omnia Beker   +3 more
doaj   +1 more source

Nucleic Acid Specificity, Cellular Localization and Reduced Toxicities of Thiazole Orange‐Neomycin Conjugates

open access: yesChemistryOpen
Selective binding of small molecule ligands to nucleic acids with high affinity and limited toxicity remains an important goal in the development of compounds that can probe DNA or RNA in cells.
Antwine W. McFarland Jr.   +10 more
doaj   +1 more source

Thiazole-Induced Surface Passivation and Recrystallization of CH3NH3PbI3 Films for Perovskite Solar Cells with Ultrahigh Fill Factors

open access: yes, 2018
The quality of perovskite films is a crucial factor governing the photovoltaic performance of perovskite solar cells. However, perovskite films fabricated by the conventional one-step spin-coating procedure are far from ideal due to uncontrollable ...
Feng Hao (1534615)   +23 more
core   +1 more source

6-Bromo-2-methylsulfanyl-1,3-benzothiazole

open access: yesActa Crystallographica Section E, 2011
The title molecule, C8H6BrNS2, is almost planar with a dihedral angle of 0.9 (1)° between the benzene and thiazole rings. The values of the geometry-based index of aromaticity (HOMA) and the nucleus-independent chemical shift (NICS ...
Michał A. Dobrowolski   +2 more
doaj   +1 more source

1,3-Thiazole-4-carbonitrile

open access: yesIUCrData, 2021
The title compound, C4H2N2S, is a 1,3-thiazole substituted in the 4-position by a nitrile group. In the crystal, C—H...N hydrogen bonds and aromatic π–π stacking interactions are observed.
Martin J. G. Fait   +3 more
doaj   +1 more source

Lichtgesteuerte Dosierung der PPARγ‐Aktivierung Mittels Schnell Relaxierender Photoschalter

open access: yesAngewandte Chemie, EarlyView.
Um eine räumlich‐zeitliche Kontrolle der PPARγ‐Aktivität zu ermöglichen, entwickelten wir den schnell relaxierenden photoschaltbaren Agonisten 6, der PPARγ selektiv in seinem lichtinduzierten Z‐Zustand aktiviert und innerhalb von Sekunden (t1/2 = 47 s) in den inaktiven E‐Zustand relaxiert.
Loris Knümann   +7 more
wiley   +1 more source

Home - About - Disclaimer - Privacy