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4-Aminocoumarin Derivatives as Multifaceted Building Blocks for the Development of Various Bioactive Fused Coumarin Heterocycles: A Brief Review
P Patra, S Patra - Current Organic Chemistry, 2022 - benthamdirect.com
Aminocoumarins are found to be present in many natural products, pharmaceuticals, and
organic materials. These derivatives demonstrate numerous biological activities including …
organic materials. These derivatives demonstrate numerous biological activities including …
Structural evolution and translational potential for agonists and antagonists of endosomal toll-like receptors
Toll-like receptors (TLRs) are members of a large family of evolutionarily conserved pattern
recognition receptors (PRRs), which serve as key components of the innate immune system …
recognition receptors (PRRs), which serve as key components of the innate immune system …
A Brief Review on the Design, Synthesis and Biological Evaluation of Pyrazolo[c]coumarin Derivatives
S Patra, P Patra - Polycyclic Aromatic Compounds, 2024 - Taylor & Francis
Both pyrazole and coumarin moiety are important scaffolds for their natural occurrences as
well as a broad spectrum of pharmaceutical properties. When coumarin fuses with pyrazole …
well as a broad spectrum of pharmaceutical properties. When coumarin fuses with pyrazole …
Design and synthesis of N-aryl-2-trifluoromethyl-quinazoline-4-amine derivatives as potential Werner-dependent antiproliferative agents
H Li, J Yu, G Yu, S Cheng, H Wu, J Wei, C You, K Liu… - Molecular Diversity, 2024 - Springer
To discover new Werner (WRN) helicase inhibitors, a series of N-aryl-2-trifluoromethyl-
quinazoline-4-amine derivatives were designed and synthesized through a structural …
quinazoline-4-amine derivatives were designed and synthesized through a structural …
Synthesis of imidazolocoumarins by the amide-directed oxidative cyclisation of enol-Ugi derivatives
JL Ramiro, AG Neo, CF Marcos - Organic & Biomolecular Chemistry, 2022 - pubs.rsc.org
The oxidative C (sp3)–H intramolecular imination of hydroxycoumarin enol-Ugi adduct
derivatives affords selectively diversely substituted imidazolocoumarins in one pot. The …
derivatives affords selectively diversely substituted imidazolocoumarins in one pot. The …
[HTML][HTML] Synthesis of highly functional quinazolins via metal-free, visible-light-enabled radical cascade arylation/cyclization of fluorinated imidoyl isothiocyanates
Y Liang, W Du, X Zeng, T **ao, Y Jiang - Green Synthesis and Catalysis, 2024 - Elsevier
A metal-free, efficient and easy-to-hand protocol for the synthesis of 2-
perfluoroalkylquinazolins has been achieved by Eosin B catalyzed radical cascade …
perfluoroalkylquinazolins has been achieved by Eosin B catalyzed radical cascade …
Structural Optimization and Biological Evaluation of Isoxazolo[5,4-d]pyrimidines as Selective Toll-Like Receptor 7 Agonists
N Strašek Benedik, A Dolšak, U Švajger… - ACS …, 2024 - ACS Publications
Toll-like receptors (TLRs) are components of innate immunity that play a crucial role in
several diseases, including chronic inflammatory and infectious diseases, autoimmune …
several diseases, including chronic inflammatory and infectious diseases, autoimmune …
Conjugate of ibrutinib with a TLR7 agonist suppresses melanoma progression and enhances antitumor immunity
S Ren, X Wang, G ** - International journal of biological …, 2022 - pmc.ncbi.nlm.nih.gov
The use of large molecules for immunotherapy has led to exciting developments in cancer
treatment, such as the development of PD-1/PD-L1 antibodies. However, small molecule …
treatment, such as the development of PD-1/PD-L1 antibodies. However, small molecule …
[HTML][HTML] Studies towards the Design and Synthesis of Novel 1,5-Diaryl-1H-imidazole-4-carboxylic Acids and 1,5-Diaryl-1H-imidazole-4-carbohydrazides as Host …
Two targeted sets of novel 1, 5-diaryl-1 H-imidazole-4-carboxylic acids 10 and
carbohydrazides 11 were designed and synthesized from their corresponding ester …
carbohydrazides 11 were designed and synthesized from their corresponding ester …
Synthesis of 2‐Perfluoroalkylazuleno[2,1‐d]pyrimidin‐4(3H)‐ones via Brønsted Acid‐Mediated Intramolecular Cyclization and Transformation into Pyrimidines
T Shoji, Y Ariga, N Sakata, D Ando… - Advanced Synthesis …, 2023 - Wiley Online Library
Brønsted acid‐mediated intramolecular cyclization of 2‐amidoazulene derivatives, prepared
by the reaction of 1‐cyano‐2‐aminoazulene derivatives with perfluoroalkyl acid anhydrides …
by the reaction of 1‐cyano‐2‐aminoazulene derivatives with perfluoroalkyl acid anhydrides …