Synthesis of 2-anilinobenzimidates, anthranilamides, and 2,3-dihydroquinazolin-4(1H)-ones from N-heterocyclic carbenes of indazole
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[1] M. Nieger,et al. Sydnone anions and abnormal N-heterocyclic carbenes of O-ethylsydnones. Characterizations, calculations and catalyses. , 2014, Chemical communications.
[2] Samantha Dodbele,et al. Species Differences in Alternative Substrate Utilization by the Antibacterial Target Undecaprenyl Pyrophosphate Synthase , 2014, Biochemistry.
[3] D. Zhang-Negrerie,et al. Intramolecular metal-free oxidative aryl-aryl coupling: an unusual hypervalent-iodine-mediated rearrangement of 2-substituted N-phenylbenzamides. , 2014, Angewandte Chemie.
[4] V. Snieckus,et al. Beyond directed ortho metalation: ruthenium-catalyzed amide-directed C(Ar)-N activation/C-C coupling reaction of anthranilamides with organoboronates. , 2014, Organic letters.
[5] S. Ji,et al. Palladium-catalyzed one-pot synthesis of quinazolinones via tert-butyl isocyanide insertion. , 2014, The Journal of organic chemistry.
[6] M. Nieger,et al. Dimerisation, rhodium complex formation and rearrangements of N-heterocyclic carbenes of indazoles , 2014, Beilstein journal of organic chemistry.
[7] F. Shi,et al. Arynes double bond insertion/nucleophilic addition with vinylogous amides and carbodiimides. , 2014, The Journal of organic chemistry.
[8] U. Bhadra,et al. Novel anthranilamide-pyrazolo[1,5-a]pyrimidine conjugates modulate the expression of p53-MYCN associated micro RNAs in neuroblastoma cells and cause cell cycle arrest and apoptosis. , 2013, Bioorganic & medicinal chemistry letters.
[9] Michael P. Storz,et al. Structure optimization of 2-benzamidobenzoic acids as PqsD inhibitors for Pseudomonas aeruginosa infections and elucidation of binding mode by SPR, STD NMR, and molecular docking. , 2013, Journal of medicinal chemistry.
[10] Zong‐Jie Guan,et al. Pericyclic rearrangements of N-heterocyclic carbenes of indazole to substituted 9-aminoacridines. , 2013, Organic & biomolecular chemistry.
[11] Jigar S. Patel,et al. Synthesis and structure-activity relationship of potent, selective and orally active anthranilamide-based factor Xa inhibitors: application of weakly basic sulfoximine group as novel S4 binding element. , 2012, European journal of medicinal chemistry.
[12] J. Baell,et al. ω-Conotoxin GVIA Mimetics that Bind and Inhibit Neuronal Cav2.2 Ion Channels , 2012, Marine drugs.
[13] Zong‐Jie Guan,et al. Mesomeric Betaines and N-Heterocyclic Carbenes of Pyrazole and Indazole , 2012 .
[14] J. Rohr,et al. Pyramidamycins A-D and 3-Hydroxyquinoline-2-carboxamide; Cytotoxic Benzamides from Streptomyces sp. DGC1 , 2012, The Journal of Antibiotics.
[15] A. Rahimi,et al. A versatile catalyst system for Suzuki-Miyaura syntheses of sterically hindered biaryls employing a cyclobutene-1,2-bis(imidazolium) salt. , 2010, Chemical communications.
[16] A. Schmidt,et al. Functionalized 4-aminoquinolines by rearrangement of pyrazole N-heterocyclic carbenes. , 2010, Angewandte Chemie.
[17] A. Schmidt,et al. N-Heterocyclic Carbenesof Indazole: Ring Enlargement Reactions by α-HaloKetones and Dehalogenations of Vicinal Dihalides , 2008 .
[18] G. Sheldrick. A short history of SHELX. , 2008, Acta crystallographica. Section A, Foundations of crystallography.
[19] Takayoshi Suzuki,et al. 2‐Anilinobenzamides as SIRT Inhibitors , 2006, ChemMedChem.
[20] Jieping Zhu,et al. Exploiting the dual reactivity of o-isocyanobenzamide: three-component synthesis of 4-imino-4H-3,1-benzoxazines. , 2005, Organic letters.
[21] A. Schmidt,et al. Synthesis of alkoxy-substituted pyridines from mono- and tricationic pyridinium salts , 2005 .
[22] A. Habeck. Nucleophilic Carbenes of Pyrazoles Starting from Pseudo-Cross-Conjugated Mesomeric Betaines , 2005 .
[23] Varinder K. Aggarwal,et al. Science of Synthesis , 2005 .
[24] A. Perosa,et al. Reaction of functionalized anilines with dimethyl carbonate over NaY faujasite. 3. chemoselectivity toward mono-N-methylation. , 2003, The Journal of organic chemistry.
[25] A. Schmidt,et al. Synthesis of new pyridines with oligocations and oxygen nucleophiles. , 2002, Organic letters.
[26] R. Whitby,et al. Palladium-catalysed synthesis of imidates, thioimidates and amidines from aryl halides , 2001 .
[27] M. Gütschow,et al. Regioselective Preparation of 1-(Bromomethyl)-5H-thiazolo[3,2-a]quinazolin-5-ones and Analogous 5H-Thieno[3,2-e]thiazolo[3,2-a]pyrimidin-5-ones from Fused 2-(Alkenylthio)pyrimidin-4-ones , 2000 .
[28] J. Lehn,et al. Janus molecules: Synthesis of double-headed heterocycles containing two identical hydrogen bonding arrays , 1994 .
[29] H. Wamhoff,et al. Pyrimido[4,5-d]pyrimidines, pyrimido[4', 5':4,5]pyrimido[6,1-a]azepines, and an imidazo[5,1-f][1,2,4]triazine by three component reaction , 1993 .
[30] K. Isogai,et al. The mechanism of the chapman rearrangement of N‐arylbenzimidate on the basis of the molecular structure established by X‐ray. Part II , 1988 .
[31] M. Kimura. Mechanism of the Chapman rearrangement of N-arylbenzimidates on the basis of a molecular structure established by X-ray crystallography , 1987 .
[32] J. Lehmann,et al. Zur reduzierenden Spaltung von Chinazolin‐2,4‐dionen On the Reductive Cleavage of Quinazoline‐2,4‐diones , 1982 .
[33] R. Barbuch,et al. A NOVEL OXAMIDE REARRANGEMENT , 1980 .
[34] J. Rowe. THE PREPARATION OF ARYL IMIDATES AND DIAROYLAMIDES BY PHASE-TRANSFER CATALYSIS , 1980 .
[35] G. Coppola,et al. Novel heterocycles. 2. Synthesis of the 1,3,2‐benzodiazaphosphorin ring system , 1978 .
[36] B. Danielsson,et al. Mass spectrometric investigation of isomeric 1,2,3,4-tetrahydro-4-oxoquinazolines , 1972 .
[37] O. Wheeler,et al. Preparation of diphenylamines via the Chapman rearrangement , 1969 .
[38] A. Chatterjee,et al. CONSTITUTION AND SYNTHESIS OF GLYCOSIN, THE NEW ALKALOID OF GLYCOSMIS PENTAPHYLLA, RETZ. DC. , 1953 .