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Molecules | Free Full-Text | Processing of Biomass Prior to Hydrogen Fermentation and Post-Fermentative Broth Management
Frontiers | Altered Cholesterol Homeostasis in Huntington's Disease
Development of Endocannabinoid-Based Chemical Probes for the Study of Cannabinoid Receptors | Journal of Medicinal Chemistry
Discovery of Vaniprevir (MK-7009), a Macrocyclic Hepatitis C Virus NS3/4a Protease Inhibitor | Journal of Medicinal Chemistry
Glucopyranosylidene-spiro-imidazolinones, a New Ring System: Synthesis and Evaluation as Glycogen Phosphorylase Inhibitors by Enzyme Kinetics and X-ray Crystallography | Journal of Medicinal Chemistry
Pharmaceutics | Free Full-Text | Synthesis of Novel 1,3,4-Oxadiazole-Derived α-Aminophosphonates/α-Aminophosphonic Acids and Evaluation of Their In Vitro Antiviral Activity against the Avian Coronavirus Infectious Bronchitis Virus
Molecules | Free Full-Text | Hydrolytic Degradation and Bioactivity of Electrospun PCL-Mg-NPs Fibrous Mats
Molecules | Free Full-Text | Lignin-Based Catalysts for C–C Bond-Forming Reactions
Binary Alkoxide Ionic Liquids | ACS Sustainable Chemistry & Engineering
DDC | Free Full-Text | Xanthene Derivatives Targeting Bacterial Efflux Pumps, Quorum-Sensing, and Biofilm Formation
![PDF) 3-Nitro-2-phenyl-2-trifluoromethyl-2H-chromenes in reactions with azomethine ylides from isatins and (thia)proline: synthesis of spiro [chromeno(thia)pyrrolizidine-11,3'-oxindoles]](https://i1.rgstatic.net/publication/347040013_3-Nitro-2-phenyl-2-trifluoromethyl-2H-chromenes_in_reactions_with_azomethine_ylides_from_isatins_and_thiaproline_synthesis_of_spirochromenothiapyrrolizidine-113'-oxindoles/links/630b83e95eed5e4bd1274eaf/largepreview.png "PDF) 3-Nitro-2-phenyl-2-trifluoromethyl-2H-chromenes in reactions with azomethine ylides from isatins and (thia)proline: synthesis of spiro [chromeno(thia)pyrrolizidine-11,3'-oxindoles]")
PDF) 3-Nitro-2-phenyl-2-trifluoromethyl-2H-chromenes in reactions with azomethine ylides from isatins and (thia)proline: synthesis of spiro [chromeno(thia)pyrrolizidine-11,3'-oxindoles]
Synthesis of Semiochemicals via Olefin Metathesis | ACS Sustainable Chemistry & Engineering
Molecules | Free Full-Text | Comparison of the Determination of Some Antihypertensive Drugs in Clinical Human Plasma Samples by Solvent Front Position Extraction and Precipitation Modes
DeepDetect: Deep Learning of Peptide Detectability Enhanced by Peptide Digestibility and Its Application to DIA Library Reduction | Analytical Chemistry
Combining host and vector data informs emergence and potential impact of an Usutu virus outbreak in UK wild birds | Scientific Reports
![Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.5b03082/asset/images/acs.orglett.5b03082.social.jpeg_v03 "Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A | Organic Letters")
Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A | Organic Letters
![Discovery of Novel Spiro[3H-indole-3,2′-pyrrolidin]-2(1H)-one Compounds as Chemically Stable and Orally Active Inhibitors of the MDM2–p53 Interaction | Journal of Medicinal Chemistry](https://pubs.acs.org/cms/10.1021/acs.jmedchem.6b00900/asset/images/medium/jm-2016-009008_0028.gif "Discovery of Novel Spiro[3H-indole-3,2′-pyrrolidin]-2(1H)-one Compounds as Chemically Stable and Orally Active Inhibitors of the MDM2–p53 Interaction | Journal of Medicinal Chemistry")
Discovery of Novel Spiro[3H-indole-3,2′-pyrrolidin]-2(1H)-one Compounds as Chemically Stable and Orally Active Inhibitors of the MDM2–p53 Interaction | Journal of Medicinal Chemistry
π-Conjugated Discrete Oligomers Containing Planar and Nonplanar Aromatic Motifs | Journal of the American Chemical Society
Glucopyranosylidene-spiro-imidazolinones, a New Ring System: Synthesis and Evaluation as Glycogen Phosphorylase Inhibitors by Enzyme Kinetics and X-ray Crystallography | Journal of Medicinal Chemistry
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Molecules | Free Full-Text | Possibilities and Limitations of the Sono-Fenton Process Using Mid-High-Frequency Ultrasound for the Degradation of Organic Pollutants
Buddhist Meditation by ดร.ศานติ โบดินันท์ - Issuu
Frontiers | Effects of choline containing phospholipids on the neurovascular unit: A review
![Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.5b03082/asset/images/large/ol-2015-030828_0008.jpeg "Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A | Organic Letters")
Unified Approach to the Spiro(pyrrolidinyl-oxindole) and Hexahydropyrrolo[2,3-b]indole Alkaloids: Total Syntheses of Pseudophrynamines 270 and 272A | Organic Letters
Molecules | Free Full-Text | Transition Metal–(μ-Cl)–Aluminum Bonding in α-Olefin and Diene Chemistry
