I2-DMSO-Mediated Transannulation of Benzo[d]isoxazol-3-amine: Direct Access to 2,4,5-Substituted Pyrimidine Derivatives.
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Kai-lu Zheng | Yan‐Dong Wu | A. Wu | Shiyi Zhuang | You Zhou | Yong-xing Tang | Jin-Yi Liu | Xiang-Long Chen
[1] Jin-Tian Ma,et al. Direct Hydrodefluorination of CF3-Alkenes via a Mild SN2' Process Using Rongalite as a Masked Proton Reagent. , 2023, Organic letters.
[2] Yan‐Dong Wu,et al. I2-DMSO mediated N1/C5 difunctionalization of anthranils with aryl methyl ketones: A facile access to multicarbonyl compounds , 2022, Tetrahedron.
[3] W. Dehaen,et al. Rhodium-Catalyzed Transannulation of 4,5-Fused 1-Sulfonyl-1,2,3-triazoles with Nitriles. The Selective Formation of 1-Sulfonyl-4,5-fused Imidazoles versus Secondary C-H Bond Migration. , 2022, The Journal of organic chemistry.
[4] Bo-Cheng Tang,et al. Pd-Catalyzed Hydroxyl-Directed Cascade Hydroarylation/C-H Germylation of Nonterminal Alkenes and Aryl Iodides. , 2022, Journal of Organic Chemistry.
[5] Yan‐Dong Wu,et al. Iodine-Mediated Multicomponent Cascade Cyclization and Sulfenylation/Selenation: Synthesis of Imidazo[2,1-a]isoquinoline Derivatives. , 2022, Organic letters.
[6] Yuanhong Liu,et al. Gold(III) or Gold(I)/Lewis-Acid-Catalyzed Substitution/Cyclization/1,2-Migration Reactions of Propargyl Alcohols with 3-Amino-benzo[d]isoxazoles: Synthesis of Pyrimidine Derivatives. , 2022, Organic letters.
[7] Jiaxi Xu,et al. Catalytic Diastereospecific and Enantioselective (3 + 2) Transannulations of 1,2,3-Thiadiazoles with Strained Norbornene Derivatives. , 2022, Organic letters.
[8] Zhiqiang Feng,et al. Design, synthesis, and structure-activity relationship of PD-1/PD-L1 inhibitors with a benzo[d]isoxazole scaffold. , 2021, Bioorganic & medicinal chemistry letters.
[9] Yan‐Dong Wu,et al. Copper‐catalyzed Reaction of Anthranils with Methyl Ketones: Site‐Selective C5‐Dicarbonylation of Anthranils , 2020, Advanced Synthesis & Catalysis.
[10] Yan‐Dong Wu,et al. Direct Synthesis of 2,3-Diaroyl Quinolines and Pyridazino[4,5- b]quinolines via an I2-Promoted One-Pot Multicomponent Reaction. , 2019, Organic letters.
[11] H. Hirao,et al. Copper-Catalyzed Asymmetric Arylation of N-Heteroaryl Aldimines: Elementary Step of a 1,4-Insertion. , 2019, Angewandte Chemie.
[12] Yan‐Dong Wu,et al. Dimethyl Sulfoxide Serves as a Dual Synthon: Construction of 5‐Methyl Pyrimidine Derivatives via Four Component Oxidative Annulation , 2018 .
[13] Xu Shen,et al. Discovery and structure-activity relationships study of thieno[2,3-b]pyridine analogues as hepatic gluconeogenesis inhibitors. , 2018, European journal of medicinal chemistry.
[14] Fei Wang,et al. Highly Site-Selective Metal-Free C-H Acyloxylation of Stable Enamines. , 2018, Organic letters.
[15] R. Kempe,et al. Manganese-Catalyzed Multicomponent Synthesis of Pyrimidines from Alcohols and Amidines. , 2017, Angewandte Chemie.
[16] M. Vrabel,et al. Single-Step Formation of Pyrimido[4,5-d]pyridazines by a Pyrimidine-Tetrazine Tandem Reaction. , 2016, Organic letters.
[17] M. El-Hashash,et al. Synthesis and antimicrobial activity of some novel substituted pyridazin-3(2H)-ones containing 1,3,4-thiadiazole moiety , 2016, Medicinal Chemistry Research.
[18] Shifeng Liu,et al. Discovery of Aryl Sulfonamides as Isoform-Selective Inhibitors of NaV1.7 with Efficacy in Rodent Pain Models. , 2016, ACS medicinal chemistry letters.
[19] M. Montès,et al. Synthesis and structure-activity relationship of non-peptidic antagonists of neuropilin-1 receptor. , 2014, Bioorganic & medicinal chemistry letters.
[20] Yan Zou,et al. Synthesis and evaluation of novel azoles as potent antifungal agents. , 2014, Bioorganic & medicinal chemistry letters.
[21] P. Yogeeswari,et al. Synthesis and antimycobacterial activities of some new N-acylhydrazone and thiosemicarbazide derivatives of 6-methyl-4,5-dihydropyridazin-3(2H)-one , 2012, Medicinal Chemistry Research.
[22] E. Opas,et al. Design, synthesis and SAR of indazole and benzoisoxazole containing 4-azetidinyl-1-aryl-cyclohexanes as CCR2 antagonists. , 2011, Bioorganic & medicinal chemistry letters.
[23] R. Syed,et al. 3-amino-7-phthalazinylbenzoisoxazoles as a novel class of potent, selective, and orally available inhibitors of p38alpha mitogen-activated protein kinase. , 2008, Journal of medicinal chemistry.
[24] K. Glaser,et al. 3-amino-benzo[d]isoxazoles as novel multitargeted inhibitors of receptor tyrosine kinases. , 2008, Journal of medicinal chemistry.