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Relevant bibliographies by topics / Isoindolo[1

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Academic literature on the topic 'Isoindolo[1'

Author: Grafiati

Published: 9 March 2023

Last updated: 31 July 2025

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Journal articles on the topic "Isoindolo[1"

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Nakao, Michiyasu, Nanako Nishikiori, Akihito Nakamura, et al. "Synthesis of Sterically Protected Isoindoles from ortho-Phthalaldehyde." SynOpen 02, no. 01 (2018): 0050–57. http://dx.doi.org/10.1055/s-0036-1591932.

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o-Phthalaldehyde (OPA) reacts with O-protected tris(hydroxyalkyl)aminomethanes in the presence of 1-propanethiol to afford a novel class of stable isoindoles. Steric protection provided by the bulkiness of C 3-symmetric primary amines derived from tris(hydroxymethyl)aminomethane could be significant for the stabilization of 1-alkylthio-2-alkyl-substituted isoindoles derived from OPA. A plausible reaction mechanism is proposed to explain the formation of the isoindole and an isoindolin-1-one by-product.

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Rodríguez, Ricaurte, Omar León, Felipe Quiroga, and Jonnathan Cifuentes. "N-{2-[(3-Oxo-1,3-dihydro-2-benzofuran-1-yl)acetyl]phenyl}acetamide." Molbank 2021, no. 3 (2021): M1244. http://dx.doi.org/10.3390/m1244.

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With the aim of obtaining different derivatives belonging to the isoindolo[2,1-a]quinoline family, we have synthesized a novel N-{2-[(3-oxo-1,3-dihydro-2-benzofuran-1-yl)acetyl]phenyl}acetamide derivative by a Claisen–Smichdt-type condensation reaction in 75% yield.

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Leznoff, Clifford C., Shafrira Greenberg, Ben Khouw, and A. B. P. Lever. "The syntheses of mono- and disubstituted phthalocyanines using a dithioimide." Canadian Journal of Chemistry 65, no. 8 (1987): 1705–13. http://dx.doi.org/10.1139/v87-285.

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Hydrolysis of 5-neopentoxy-1,3-diiminoisoindoline gave 5-neopentoxy-1H-isoindole-1,3(2H)-dione (4-neopentoxyphthalimide), which, on treatment with Lawesson's reagent, yielded the thiophthalimides, 5-neopentoxy-1H-isoindole-1,3(2H)-dithione, 2,3-dihydro-6-neopentoxy-3-thioxo-1H-isoindol-1-one, and 2,3-dihydro-5-neopentoxy-3-thioxo-1H-isoindol-1-one. Attempted S-alkylations of the thiophthalimides resulted in the formation of β-isoindigos and N-alkylation products. In a new phthalocyanine synthesis crossed condensations of 1,3-diiminoisoindoline with 5-neopentoxy-1H-isoindole-1,3(2H)-dithione yi

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Odabasoglu, M., and O. Buyukgungor. "Structure of dihydro-isoindolo benzoxazine-11-one and dibromo-cyclopenta[a]naphthalene-1-one." Acta Crystallographica Section A Foundations of Crystallography 64, a1 (2008): C385. http://dx.doi.org/10.1107/s0108767308087692.

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Kraus, George A., and Hakwon Kim. "The Synthesis of Isoindolo[2, 1-a]indoles via Both Radical and Organopalladium Strategies." Synthetic Communications 23, no. 1 (1993): 55–64. http://dx.doi.org/10.1080/00397919308020401.

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Kim, Hyoung Shik, Yun Mi Chung, Young Ja Park та Jae Nyoung Kim. "ChemInform Abstract: Reinvestigation for the Synthesis of 1,2-Isoindolo-1(2H)-3,4-tetrahydro-β-carboline." ChemInform 31, № 44 (2000): no. http://dx.doi.org/10.1002/chin.200044153.

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Rosevear, J., and JFK Wilshire. "A Comparison of the Reactions of Some Ethyl N-Arylcarbamates With Those of the Corresponding Acetanilides. II. Amidomethylation With N-Hydroxy-methylphthalimide." Australian Journal of Chemistry 43, no. 2 (1990): 339. http://dx.doi.org/10.1071/ch9900339.

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The reactions of some ethyl N- arylcarbamates and of the corresponding acetanilides towards 1 equiv. of N-hydroxymethylphthalimide in concentrated sulfuric acid at 50° have been compared with one another. In the case of certain para-substituted compounds, amidomethylation occurs more readily ortho to the carbamate group than to the N-acetyl group. The diagnostic use of (D6)benzene as a 1H n.m.r. solvent, particularly for the structural elucidation of the ortho-( phthalimidomethyl )- phenylcarbamates and -acetanilides, is reported. Acidic treatment of the ortho -( phthalimidomethyl ) phenylcarb

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Tkachuk, V., T. Lyubchuk, T. Tkachuk, and O. Hordiyenko. "A DEVELOPMENT OF AN EFFECTIVE METHOD FOR THE SYNTHESIS OF 2-(5-OXO-4,5-DIHYDRO-1,2,4-OXADIAZOL-3-YL)BENZOIC ACID." Bulletin of Taras Shevchenko National University of Kyiv. Chemistry, no. 1 (57) (2020): 51–54. http://dx.doi.org/10.17721/1728-2209.2020.1(57).13.

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2-(5-Oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzoic acid was synthesized using a new effective method – thermal heterocyclization of 3-(hydroxyimino)isoindolin-1-one, which occurs as a result of its interaction with 1,1'-carbonyldiimidazole (CDI) and subsequent base-promoted cycleopening of the obtained intermediate 3H,5H-[1,2,4]oxadiazolo[3,4-a]isoindole-3,5-dione. Direct cyclization of 3-(hydroxyimino)isoindolin-1-one by the reaction with diethyl carbonate in the presence of sodium ethylate in ethanol at room temperature and under heating was unsuccessful. The same result was observed when usi

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Boltukhina, E. V., F. I. Zubkov, and A. V. Varlamov. "Methods for the construction of [1,2]isoindolo-condensed benzazepines, benzazocines, quinolines, and isoquinolines. 1. Isoindolobenzazepines, isoindolobenzazocines. (Review)." Chemistry of Heterocyclic Compounds 42, no. 7 (2006): 831–57. http://dx.doi.org/10.1007/s10593-006-0169-0.

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PIGEON, P., and B. DECROIX. "ChemInform Abstract: Tetracyclic Systems: Synthesis of Isoindolo(1,2-b)thieno(2,3(3,2 or 3, 4)-e)(1,3)thiazocines and Isoindolo(2,1-a)thieno(2,3(3,2 or 3,4)-f)(1, 4) and (1,5)diazocines." ChemInform 28, no. 37 (2010): no. http://dx.doi.org/10.1002/chin.199737190.

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Dissertations / Theses on the topic "Isoindolo[1"

1

Guyenne, Sabrina. "Design and synthesis of isoindolin-1-ones inhibitors of the p53-MDM2 interaction." Thesis, University of Newcastle Upon Tyne, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.407873.

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Modolo, Isabelle. "Studies toward completion of the C1-C28 segment of spongistatin 1. Synthesis and photochemistry of 4bH-pyrido[2,1-a]isoindol-6-one." The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1236277748.

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Hsu, Sung-Lin, and 許松林. "Synthetic Applications of Sulfone-Substituted Isoindole-1-ones." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/52629436644855215016.

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碩士<br>輔仁大學<br>化學系<br>103<br>This thesis improves the synthesis of isoindol-1-one 19, and studies its synthetic applications. Treatment of compound 19 with base yielded the diene 20. The reaction of compound 20 with DDQ gave the aromatic compound 21. Oxidation of compound 20 with m-CPBA gave the epoxy compound 22. Compound 22 was treated with different nucleophiles to give compounds 23, 24, 25, 26.

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Chang, Li-Juan, and 張麗娟. "Methanolysis of 2-Alkylbenzonitriles:Synthesis of 3-Substituted-1(2H)-isoquinolone and 3-Alkylidene isoindol-1-one." Thesis, 1998. http://ndltd.ncl.edu.tw/handle/56080644089999964538.

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碩士<br>高雄醫學院<br>藥學研究所<br>86<br>The treatment of 2-(2-alkylethynyl) benzonitrile with sodium methoxide in methanol gave 3-alkyl-1(2H)-isoquinolinone in modest yield. Under the same reaction conditions methanolysis of 2-(2-arylethynyl)benzonitrile lead to the formation of 3-alkylidene isoindol-1-one. Partial hydrolysis of 2- (1-hexynyl) benzonitrile to the corresponding benzamide, followed by the treatment of the benzamide with sodium methoxide gave 3-pentylidene isoindol-1-one in 11% yield. T

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Jäger, Ulrich [Verfasser]. "Synthese von Benzo[f]pyrido[2,1-a]isoindol-Heterocyclen durch Cycloisomerisierung von 2-Phenylethinyl-1-propargylpyridinium-Salzen / vorgelegt von Ulrich Jäger." 2005. http://d-nb.info/995069638/34.

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Chen, Bo-Fong, and 陳伯峰. "1. A Versatile Approach to 6-Substituted-5-methoxy-d-lactam Framework and Application to the Synthesis of Natural Products and Pharmaceuticals 2. A New Approach to Isoindolone Skeleton." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/54215609877262062807.

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博士<br>國立中山大學<br>化學系研究所<br>93<br>1. The key glutarimides were obtained via facile [3+3] annulation. The method featured regioselective introduction of C-6 substituents in glutarimides, and application to the synthesis of natural products and pharmaceuticals. 2. The synthesis of a novel substituted aza-ticyclic compounds through the use of the intramolecular Diels-Alder reaction is present. Further aromaticzation in the present of BF3 to afford 2,3-dihydro-isoindolone.The use of method for the rapid preparation of a substituted isoindolone framework is described.

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Book chapters on the topic "Isoindolo[1"

1

Donohoe, T. J. "Formation of Isoindole-1-carbonitrile From a Dipole." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00822.

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Jeevithan, Lakshmi, Jeevithan Elango, Jose Eduardo Mate Sanchez De Val, and Wenhui Wu. "Marine-Derived Novel Compounds for Fibrinolysis." In Biochemistry. IntechOpen, 2024. https://doi.org/10.5772/intechopen.115095.

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Marine-derived natural compounds play a major role in treating several human-related diseases due to their unique chemical diversity, biocompatibility, and excellent medicinal properties. Recent studies have explored the potential of marine organisms, especially microorganisms, as sources for novel bioactive substances that possess fibrinolytic activity. For the past decades, our team has been exploring marine-derived secondary metabolites as novel compounds for thrombolysis and fibrinolysis. Our recent studies investigated the fibrinolytic properties of Fungi fibrinolytic compound(R)-2,5-bis(

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3

Meigh, J. P. K. "From 2-(1a,2,7,7a-Tetrahydro-1-naphtho[2,3-]aziren-1-yl)-1-isoindole-1,3(2)-dione." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01327.

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Conference papers on the topic "Isoindolo[1"

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Arjunan, V., I. Saravanan, P. Ravindran, S. Mohan, P. M. Champion, and L. D. Ziegler. "Structural, Vibrational and DFT Studies on 2-chloro-1H-isoindole-1, 3(2H)-dione and 2-methyl-1H-isoindole-1, 3(2H)-dione." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482382.

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Iskandar, F., A. H. Jahidin, I. Abdul Wahab, and H. H. Mizaton. "Suggesting a derivative of isoindol-1-one from a Vitex species." In 2010 International Conference on Science and Social Research (CSSR). IEEE, 2010. http://dx.doi.org/10.1109/cssr.2010.5773756.

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Merchán Arenas, D. R., and V. V. Kouznetsov. "The use of isoprene as a dienophile in stereo- regioselective synthesis of new isoindolo[2,1-a]quinolin-11(5H)-ones via PMA-catalyzed three component Povarov reaction." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0378-1.

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