An Efficient Synthesis of Phthalimides and Their Biological Activities

References

• V. Pace, F. Martínez, C. I. Nova, M. Fernández, J. V. Sinisterra, and A. R. Alcántara, “Efficient Horner–Wadsworth–Emmons Intramolecular Cyclisation of a N-Substituted Phthalimide Promoted by KF-Alumina: A General Tool for the Synthesis of Functionalised Isoindolinones,” Tetrahedron Letters.50, no. 25 (2009): 3050–3.
   Web of Science ®Google Scholar
• M. Lamblin, A. Couture, E. Deniau, and P. Grandclaudon, “Alternative and Complementary Approaches to the Asymmetric Synthesis of C3 Substituted NH Free or N-Substituted Isoindolin-1-One,” Tetrahedron: Asymmetry. 19, no. 1 (2008): 111–23.
   Google Scholar
• Y. Nozawa, M. Ito, K. Sugawara, K. Hanada, and K. Mizoue, “Stachybotrin C and Parvisporin, Novel Neuritogenic Compounds. II. Structure Determination,” The Journal of Antibiotics 50, no. 8 (1997): 641–5.
   PubMed Web of Science ®Google Scholar
• L. A. Sorbera, P. A. Leeson, J. Silvestre, and J. Castaner, “Drugs Future,” Journals on the Web 26 (2001): 651.
   Google Scholar
• J. C. Breytenbach, S. V. Dyk, I. V. D. Heever, S. M. Allin, C. C. Hodkinson, C. J. Northfield, and M. I. Page, “Synthesis and Antimicrobial Activity of Some Isoindolin-1-Ones Derivatives,” Bioorganic & Medicinal Chemistry Letters 10, no. 15 (2000): 1629–31.
   PubMed Web of Science ®Google Scholar
• C. Maugeri, M. A. Alisi, C. Apicella, L. Cellai, P. Dragone, E. Fioravanzo, S. Florio, G. Furlotti, G. Mangano, R. Ombrato, et al. “New anti-Viral Drugs for the Treatment of the Common Cold,”Bioorganic & Medicinal Chemistry 16, no. 6 (2008): 3091–107.
   PubMed Web of Science ®Google Scholar
• X. Z. Zhao, K. Maddali, C. Marchand, Y. Pommier, and T. R. Burke, “Diketoacid-Genre HIV-1 Integrase Inhibitors Containing Enantiomeric Arylamide Functionality,” Bioorganic & Medicinal Chemistry 17no. 14 (2009): 5318–24.
   PubMed Web of Science ®Google Scholar
• Tetsuro Shirasaka, Takato Kunitake, and Isao Tsuneyoshi, “Cardiovascular Responses to Intravenous Injection of a Novel Isoindolin-1-One Derivate in Conscious Rats,” Brain Research 1300, (2009): 105–13.
   PubMed Web of Science ®Google Scholar
• Guertin K. R. (2002) US Patent 6482951 (B2)
   Google Scholar
• Arakawa K, Nishimura T, Sugimoto Y, Takahashi H, Shimamura T. (2013) US Patent 8362052 (B2)
   Google Scholar
• (a) Frank A J, Man H W, Ge C, Saindane M. (2013) US Patent 8415485 (B2);
   Google Scholar
  (b) Willems H M G, Kallblad P, Hardcastle I R, Griffin R J, Golding B T, Lunec J, Noble M E M, Newell D R, Calvert A H. (2012) US Patent 8258175 (B2);
   Google Scholar
  (c) Dally R. D, Woods T A. (2014) US Patent 0275121 (A1)
   Google Scholar
• (a) Zhao P L, Ma W F, Duan A N, Zou M, Yan Y C, You W W, Wu S G. (2012) “An Accurate Calculation of the Elongation of Strip in Tension Leveling Process,” Archiv der Pharmazie, 7(345):509–822;
   Google Scholar
  (b) Ignasik M, Bajda M, Guzior N, Prinz M, Holzgrabe U, Malawska B. (2012 ) “Synthesis and Evaluation of Novel 2-(aminoalkyl)-isoindoline-1,3-dione derivatives as Dual-binding Site Acetylcholinesterase Inhibitors,” Arch Pharm Chem Life Sci (345): 509–516;
   PubMed Web of Science ®Google Scholar
  (c) Lindsley C W, Conn P J, Wood M R, Hopkins C R, Melancon B J, Poslusney M S, Engers D W. (2014) US Patent 2014/0288084 (A1);
   Google Scholar
  (d) Meltzer H Y, Horiguchi M. (2014)US Patent 8,735,397 (B2)
   Google Scholar
• (a) Dubois V, Van Ginneken C, De Cock H, Lambeir A. M, Van der Veken P, Augustyns K, Chen X, Scharpé S, De Meester, I J. (2009) “Enzyme Activity and Immunohistochemical Localization of Dipeptidyl Peptidase 8 and 9 in Male Reproductive Tissues,” The Journal of Histochemistry and Cytochemistry, 6(57): 531–541;
   Google Scholar
  (b) Jiaang W T, Chen Y S, Hsu T, Wu S. H, Chen, C H, Chang C N, Chang C N, Lee S J, Chen X. (2005) “Novel Isoindoline Compounds for Potent and Selective Inhibition of Prolyl Dipeptidase DPP8,” Bioorganic & Medicinal Chemistry Letters (15); 687–691
   PubMed Web of Science ®Google Scholar
• P. Stevenson, H. McAlonan, J. P. Murphy, M. Nieuwenhuyzen, K. Reynolds, P. K. S. Sarma, and N. J. Thompson, “ChemInform Abstract: 4-Phenyloxazolidin-2-Ones and Isoindolin-1-Ones: Chiral Auxiliaries for Diels-Alder Reactions of N-Substituted 1,3-Dienes,” Cheminform 33no. 21 (2010): no–79. ():
   Google Scholar
• (a) Miyabe H, Yoshida K, Kobayashi Y, Matsumura A, Takemoto Y. (2003) Synthesis of “Azacycles Based on Iridium-Catalyzed Sequential Allylic Amination,” Synlett 1031–1033;
   Google Scholar
  (b) Stajer G, Csende F. (2005) Advanced Methods for the Synthesis of 3-Substituted 1H-Isoindol-1-Ones. Current Organic Chemistry (9): 1277–1286;
   Web of Science ®Google Scholar
  (c) Buchert M, Meinke S, Prenzel A, Deppermann N, Maison W. (2006) Azabicycloalkenes as Synthetic Intermediates − Synthesis of Azabicyclo[X.3.0]alkane Scaffolds. Organic Letters (8): 5553–5556
   PubMed Web of Science ®Google Scholar
• (a) T. J. Donohoe, “Product class 14: 1H- and 2H isoindoles,” Science of Synthesis 10, (2001): 653–692;
   Google Scholar
  (b) Bonnett R, North S. A., “The Chemistry of the Isoindoles,” Advances in Heterocyclic Chemistry 29, (1981): 341–399.
   Google Scholar
• Le. Pan, Xiuzhuang. Li, Chengwen. Gong, Hui. Jin, and Bo. Qin, “Synthesis of N-Substituted Phthalimides and Their Antifungal Activity Against Alternaria Solani and Botrytis Cinerea,”Microbial Pathogenesis 95 (2016): 186–92.
   PubMed Web of Science ®Google Scholar
• G. Petranyi, J. G. Meingassner, and H. Mieth, “Antifungal Activity of the Allylamine Derivative Terbinafine in Vitro,” Antimicrobial Agents and Chemotherapy 31, no. 9 (1987): 1365–8.
   PubMed Web of Science ®Google Scholar
• Kai Li, Xinbo Fu, Yanan Zhao, Wentao Gao, and Yang Li, “A Facile Synthesis of Novel Pyrrolo[3,4-b]Quinolin-1-One Derivatives,” Research on Chemical Intermediates 42, no. 5 (2016): 4273–87.
   Web of Science ®Google Scholar