Results 191 to 200 of about 10,094 (251)
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Surface-induced dimerization of 2-thiazoline-2-thiol on silver and gold nanoparticles: A surface enhanced Raman scattering (SERS) and density functional theoretical (DFT) study

, 2020
The adsorption behavior of an anti-thyroid agent, 2-thiazoline-2-thiol (TT) on silver (Ag) and gold (Au) nanoparticles (NPs) was studied using surface enhanced Raman scattering (SERS) and density functional theory (DFT).
Ridhima Chadha   +3 more
semanticscholar   +1 more source

D3-Thiazolines, D4-Thiazolines and Thiazoles from Penem Antibiotics

HETEROCYCLES, 1992
Upon cleavage of the β-lactam ring, penems are converted to unstable Δ 4 -thiazolines, which epimerize at the ex-C-5 position, lose a nucleofugal group at C-2' (if originally present), tautomerize to Δ 3 -thiazolines, or suffer hydrolytic decomposition.
Ugo Chiacchio   +8 more
openaire   +1 more source

One-Pot Synthesis of Benzimidazo[2,1-b]thiazoline Derivatives through An Addition/Cyclization/Oxidative Coupling Reaction.

Journal of Organic Chemistry, 2020
A novel and efficient approach to the synthesis of benzimidazo[2,1-b]thiazoline derivatives has been developed through an addition/cyclization/intramolecular oxidative C-H functionalization process.
Haofeng Wang   +9 more
semanticscholar   +1 more source

Thiazoline carboxylic acid from formylcysteine

Experientia, 1957
La formilcisteina in HCl 12N da un assorbimento nell'ultravioletto indicante la formazione di un anello tiazolinico. La reazione e piu rapida per la formilcisteina che per il glutatione e dipende dalla concentrazione dell'acido. Trattando la formicilsteina con HCl 12N, e stato preparato un composto avente le proprieta dell'acido tiazolin carbossilico ...
D, CAVALLINI, B, MONDOVI, C, DE MARCO
openaire   +2 more sources

Infrarotspektren einiger Thiazoline

Chemische Berichte, 1955
AbstractDie Infrarotspektren von 15 in 2‐Stellung substituierten Thiazolinen wurden aufgenommen. Folgende charakteristische Frequenzen treten auf: a) 6.1–6.45 μ (stark), b) 8.0–8.4 μ (mittelstark bis schwach) und c) 9.8–10.5 μ (stark). Thiazole absorbieren im Bereich a) (6.1–6.45 μ) nur schwach, Thiazolidine nicht.
Otting, W., Drawert, F.
openaire   +2 more sources

Thiazoline-pyrene selective and sensitive fluorescence "turn-on" sensor for detection of Cu2.

Spectrochimica Acta Part A - Molecular and Biomolecular Spectroscopy, 2019
A thiazoline and pyrene containing sensor 1 was synthesized via one-pot reaction and utilized as a highly selective and sensitive fluorescence "turn-on" sensor for Cu2+ detection, via the fluorescence enhancement of pyrene monomer emission.
Jing Wang   +8 more
semanticscholar   +1 more source

Tautomeric Modification of GlcNAc-Thiazoline

Organic Letters, 2007
The potent O-GlcNAcase (OGA) inhibitor GlcNAc-thiazoline has been modified by buffer- or acylation-induced imine-to-enamine conversion and then electrophile or radical addition (Xn = D3, F, N3, OH, SMe, COCF3, CF3). Several functionalized GlcNAc-thiazolines show highly selective inhibition of OGA vs human hexosaminidase and thus have promise as tools ...
Spencer, Knapp   +6 more
openaire   +2 more sources

2‐Acetonyl‐thiazolin

Chemische Berichte, 1953
AbstractAus 2‐Methyl‐thiazolin und Keten wird 2‐Acetonyl‐thiazolin erhalten, das mit Kupfersalzen eine Komplex‐Verbindung liefert und im Rattenschwanz‐Test blutdrucksenkend wirkt.
Richard Kuhn   +2 more
openaire   +1 more source

ChemInform Abstract: δ3‐Thiazolines, δ4‐Thiazolines, and Thiazoles from Penem Antibiotics.

ChemInform, 1992
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
G. VISENTIN   +8 more
openaire   +1 more source

Synthesis and antioxidant activity of pyrazolyl-oxazolines/thiazolines and isoxazolyl-oxazolines/thiazolines

Medicinal Chemistry Research, 2013
A new class of pyrazolyl/isoxazolyl-oxazolines and thiazolines were synthesized from E-arylsulfonylethenesulfonylacetic acid methyl ester and tested for antioxidant activity. Among the tested compounds, 14b exhibited excellent antioxidant activity when compared with the standard ascorbic acid.
Adivireddy Padmaja   +4 more
openaire   +1 more source

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