Results 61 to 70 of about 1,179 (184)
Antidiabetic and Cytotoxicity Studies of Novel Quinazolinone–1,3,4‐Thiadiazole Molecular Hybrids
ABSTRACT In the treatment of diabetes mellitus (DM), inhibition of carbohydrate‐hydrolysing enzymes, such as α‐amylase, has emerged as a promising therapeutic strategy. In the present study, a series of quinazolinone‐1,3,4‐thiadiazole molecular hybrids were designed, synthesized and biologically evaluated for their antidiabetic potential.
Prishani Kisten +9 more
wiley +1 more source
Thiosemicarbazones were evaluated for antidiabetic activity via α‐amylase inhibition. Compound 6g showed two‐fold greater potency than acarbose. Benzaldehyde‐ and ketone‐derived analogues were most active, while isatin and furan derivatives were less effective. Several compounds displayed antioxidant activity. Docking highlighted hydrogen bonding and π–
Neha Manhas +9 more
wiley +1 more source
A One-Pot Divergent Sequence to Pyrazole and Quinoline Derivatives
The hydroxy-pyrazole and 3-hydroxy-oxindole motifs have been utilised in several pharma and agrochemical leads but are distinctly underrepresented in the scientific literature due to the limited routes of preparation.
Guido Gambacorta +2 more
doaj +1 more source
Five isatin anions were prepared by deprotonation of initial isatins in aprotic solvents using basic fluoride and acetate anions (F− and CH3COO−). The F− basicity is sufficient to deprotonate isatin NH hydrogen from all the studied compounds.
Pavol Tisovský +9 more
doaj +1 more source
Expanding the chemical diversity of spirooxindoles via alkylative pyridine dearomatization
A mild and practical synthesis of spirooxindole [1,3]oxazino derivatives from N-substituted isatins and 1,3-dicarbonyl compounds with pyridine derivatives is reported. The reactions provided good to excellent yields.
Chunhui Dai +2 more
doaj +1 more source
Chiral binaphthyl-modified squaramide-catalyzed enantioselective addition of diphenyl phosphonate to ketimines derived from isatins has been achieved. This method affords practical and efficient access to chiral 3-amino-3-phosphonyl-substituted oxindole ...
Hee Seung Jang, Yubin Kim, Dae Young Kim
doaj +1 more source
Molecular Iodine: A Powerful Catalyst for the Knoevenagel Condensation of Isatins with Malononitrile
Molecular iodine has been used as an efficient catalyst for an improved and rapid condensation of isatins with malononitrile in excellent yields. The significant features of the iodine-catalyzed Knoevenagel condensation are operational simplicity ...
Xiao Juan Yang, Yong Sen Zhang
doaj +1 more source
The one-pot four-component reaction of benzohydrazide (2-picolinohydrazide), acetylenedicarboxylate, isatins and malononitrile (ethyl cyanoacetate) with triethylamine as base catalyst afforded functionalized 1-benzamidospiro[indoline-3,4'-pyridines] in ...
Chao Wang, Yan-Hong Jiang, Chao-Guo Yan
doaj +1 more source
Spectroscopic studies on Isatin-3-Semicarbazone and Isatin-3-Thiosemicarbazone
The configurations of semi-and thiosemicarbazone derivatives of isatin are assigned by means of 1H and 13C NMR Spectroscopy including NOE difference spectra, IR and electronic spectral data of these compounds are also reported and discussed. The electron impact (EI), fast atom bombardment (FAB) and negative ion chemical ionization (NICI) mass spectra ...
openaire +3 more sources
Organocatalytic asymmetric allylic amination of Morita–Baylis–Hillman carbonates of isatins
The investigation of a Lewis base catalyzed asymmetric allylic amination of Morita–Baylis–Hillman carbonates derived from isatins afforded an electrophilic pathway to access multifunctional oxindoles bearing a C3-quaternary stereocenter, provided with ...
Hang Zhang +4 more
doaj +1 more source

