GIAMMARCO
TENTI
Chercheur dans le période 2011-2016
Publications (17) Publications de GIAMMARCO TENTI
2022
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An Efficient Synthesis of a Highly Functionalized DihydrobenzoÂthiophene Derivative: A Ring-Contracted Analogue of the Anti-inflammatory Drug Propoxicam
Synlett, Vol. 33, Núm. 15, pp. 1500-1504
2021
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(E)-3-((2-Fluorophenyl)(hydroxy)methylene)imidazo[1, 2-a]pyridin-2(3H)-one
MolBank, Vol. 2021, Núm. 2
2020
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Antioxidant, anti-inflammatory and neuroprotective profiles of novel 1,4-dihydropyridine derivatives for the treatment of alzheimer’s disease
Antioxidants, Vol. 9, Núm. 8, pp. 1-20
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Aza-CGP37157-lipoic hybrids designed as novel Nrf2-inducers and antioxidants exert neuroprotection against oxidative stress and show neuroinflammation inhibitory properties
Drug Development Research, Vol. 81, Núm. 3, pp. 283-294
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Synthesis of 1,4-Diazepanes and Benzo[ b][1,4]diazepines by a Domino Process Involving the in Situ Generation of an Aza-Nazarov Reagent
Journal of Organic Chemistry, Vol. 85, Núm. 18, pp. 11924-11933
2017
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Addition to "ITH14001, a CGP37157-Nimodipine Hybrid Designed to Regulate Calcium Homeostasis and Oxidative Stress, Exerts Neuroprotection in Cerebral Ischemia"
ACS chemical neuroscience, Vol. 8, Núm. 1, pp. 210
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Discovery of the first dual GSK3β inhibitor/Nrf2 inducer. A new multitarget therapeutic strategy for Alzheimer's disease
Scientific Reports, Vol. 7
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ITH14001, a CGP37157-Nimodipine Hybrid Designed to Regulate Calcium Homeostasis and Oxidative Stress, Exerts Neuroprotection in Cerebral Ischemia
ACS Chemical Neuroscience, Vol. 8, Núm. 1, pp. 67-81
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Synthesis of pyridines by multicomponent reactions
Multicomponent Reactions: Synthesis of Bioactive Heterocycles (CRC Press), pp. 1-32
2016
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Mejoría de la glicosilación para optimizar la producción de anticuerpos monoclonales
Actualidad en farmacología y terapéutica, Vol. 14, Núm. 3, pp. 233-235
2015
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Six-membered heterocycles
Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis (wiley), pp. 45-86
2014
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A heavy metal- and oxidant-free, one-pot synthesis of pyridines and fused pyridines based on a Lewis acid-catalyzed multicomponent reaction
Chemical Communications, Vol. 50, Núm. 82, pp. 12270-12272
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New 5-unsubstituted dihydropyridines with improved CaV1.3 selectivity as potential neuroprotective agents against ischemic injury
Journal of Medicinal Chemistry, Vol. 57, Núm. 10, pp. 4313-4323
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Ruthenium(II)-catalyzed oxidative C-H alkenylations of sulfonic acids, sulfonyl chlorides and sulfonamides
Chemistry - A European Journal, Vol. 20, Núm. 46, pp. 15248-15251
2013
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A new multicomponent protocol for the synthesis of pyridines and fused pyridines via a formal aza [3+3] cycloaddition
Current Organic Synthesis, Vol. 10, Núm. 4, pp. 645-654
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Identification of 4,6-diaryl-1,4-dihydropyridines as a new class of neuroprotective agents
MedChemComm, Vol. 4, Núm. 3, pp. 590-594
2012
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One-pot access to a library of structurally diverse nicotinamide derivatives via a three-component formal Aza [3 + 3] cycloaddition
ACS Combinatorial Science, Vol. 14, Núm. 10, pp. 551-557