Фураны в синтезе азагетероциклов, страница 78

M. Campbell, N. Cosford, L.Zongli, M. Sainsbury // Tetrahedron – 1987. – V. 43. – № 6. – P. 1117–1122.349. Couture A. An Expeditious Synthesis of 3-Alkyl-, Aryl- and Heteroaryl-indoles by Way ofan Intramolecular Horner-Wittig Reaction / A. Couture, E. Deniau, Y. Gimbert, P. Grandclaudon // J. Chem. Soc.

Perkin Trans. 1 – 1993. – P. 2463–2466.350. Katritzky A. R. Facile synthesis of benzotriazines and indoles by ring-scissions of α-benzotriazol-1-yl hydrazones / A. R. Katritzky, J. Wang, N. Karodia, J. Li // Synth. Commun. –1997. – V. 27. – № 22. – P. 3963–3976.351. Miyagi T. New synthesis of 3-substituted indoles using lithium trimethylsilyldiazomethane/ T. Miyagi, Y. Hari, T. Aoyama // Tetrahedron Lett.

– 2004. – V. 45. – № 33. – P. 6303–6305.352. Nishiura M. Synthesis of 4-(azuleno[b]indolyl)-3-buten-2-ones by intramolecular tropylium ion-mediated furan ring-unravelled reaction / M. Nishiura, I. Ueda, K. Yamamura //Heterocycles – 2007. – V. 74. – № C. – P. 951–960.353. Sun C. Facile synthesis of 3-(2-furanyl)indoles via a multicomponent reaction / C. Sun, S.J. Ji, Y. Liu // Tetrahedron Lett. – 2007. – V. 48. – № 51. – P. 8987–8989.354.

Kim T. Practical method for synthesis of 2,3-disubstituted indole derivatives promoted byβ-(benzotriazol-1-yl)-allylic O-stannyl ketyl radicals / T. Kim, K. Kim // Tetrahedron Lett.– 2010. – V. 51. – № 5. – P. 868–871.374355. Reddy B. V. S. Three-Component One-Pot Synthesis of 3-(2-Furanyl)indoles from Acetylenedicarboxylates, Isocyanide, and 3-Formylindole / B. B. S. Reddy, A. M. Reddy, D.Somashekar, J.

S. Yadav, B. Sridhar // Synthesis – 2010. – № 15. – P. 2571–2576.356. Dowlut M. An Efficient Low-Temperature Stille-Migita Cross-Coupling Reaction for Heteroaromatic Compounds by Pd-PEPPSI-Ipent / M. Dowlut, D. Mallik, M. G. Organ //Chem. Eur. J. – 2010. – V. 16. – № 14. – P. 4279–4283.357. Alcaide B. Carbocyclization versus Oxycyclization on the Metal-Catalyzed Reactions ofOxyallenyl C3-Linked Indoles / B.

Alcaide, P. Almendros, J. M. Alonso, I. Fernandez // J.Org. Chem. – 2013. – V. 78. – № 13. – P. 6688–6701.358. Nishida A. Synthesis of (3-indolyl)heteroaromatics by Suzuki-Miyaura coupling and TheirInhibitory Activity in Lipid Peroxidation // Heterocycles – 2003. – V. 59. – № 2. – P.

473–476.359. Williams J. D. Design, Synthesis, and Antiviral Activity of Certain 3-Substituted 2,5,6Trichloroindole Nucleosides / J. D. Williams, J. J. Chen, J. C. Drach, L. B. Townsend // J.Med. Chem. – 2004. – V. 47. – № 23. – P. 5753–5765.360. Williams J. D. Synthesis, Antiviral Activity, and Mode of Action of Some 3-Substituted2,5,6-Trichloroindole 2- and 5-Deoxyribonucleosides / J. D. Williams, R. G. Ptak, J. C.Drach, L. B. Townsend // J. Med. Chem. – 2004. – V. 47. – № 23.

– P. 5773–5782.361. Diana P. Synthesis and antitumor activity of 2,5-bis(3-indolyl)-furans and 3,5-bis(3-indolyl)isoxazoles, nortopsentin analogues / P. Diana, A. Carbone, P. Barraja, G. Kelter, H.-H.Fiebig, G. Cirrincione // Bioorg. Med. Chem. – 2010.

– V. 18. – № 12. – P. 4524–4529.362. Бутин А. В. Полифурил(арил)алканы и их производные. 17. Синтез соединений рядаоксазулена / А. В. Бутин, А. В. Гутнов, В. Т. Абаев, Г. Д. Крапивин // ХГС – 1998. –№ 7. – c. 883–892.363. Дмитриев А. С. 2-Карбоксиарилдифурилметаны в синтезе кетонов изокумариновогоряда / А. С. Дмитриев, С. А. Поделякин, В. Т. Абаев, А. В. Бутин // ХГС – 2005. –№ 9. – c. 1400–1402.364. Barry R.

D. Isocoumarins: Developments since 1950 / R. D. Barry // Chem. Rev. – 1964. –V. 64. – № 3. – P. 229–260.365. Pal S. Isocoumarin and Its Derivatives: An Overview on their Synthesis and Applications /S. Pal, V. Chatare, M. Pal // Curr. Org. Chem. – 2011. – V. 15. – № 5. – P.

782–800.366. Meepagala, K. M. Antifungal Constituents of the Essential Oil Fraction of Artemisia dracunculus L. Var. dracunculus / K. M. Meepagala, G. Sturtz, D. E. Wedge // J. Agric. FoodChem. – 2002. – V. 50. – № 24. – P. 6989–6992.375367. Engelmeier D. Antifungal 3-Butylisocoumarins from Asteraceae-Anthemideae / D. Engelmeier, F. Hadacek, O.

Hofer, G. Lutz-Kutschera, M. Nagl, G. Wurz, H. Greger // J. Nat.Prod. – 2004. – V. 67. – № 1. – P. 19–25.368. Rama N. H. Synthesis and anti-bacterial activity of some 3-alkylisocoumarins and (±)-3-alkyl-3,4-dihydroisocoumarins / N. H. Rama, R. Iqbal, K. Zamani, A. Saeed, M.

Z. Iqbal, M.I. Chaudhary // Ind. J. Chem. – 1998. – V. 37. – № 4. – P. 365–369.369. Kumagai H. Cytogenin, a novel antitumor substance / H. Kumagai, T. Masuda, M. Ohsono, S. Hattori, H. Naganawa, T. Sawa, M. Hamada, M. Ishizuka, T. Takeuchi // J. Antibiot.– 1990. – V.

43. – № 11. – P. 1505–1507.370. Salloum R. M. NM-3, an Isocoumarin, Increases the Antitumor Effects of Radiotherapywithout Toxicity / R. M. Salloum, N. T. Jaskowiak, H. J. Mauceri, S. Seetharam, M. A.Beckett, A. M. Koons, D. M. Hari, V. K. Gupta, C. Reimer, R. Kalluri, M. C. Posner, S.Hellman, D. W. Kufe, R. R. Weichselbaum // Cancer Res. – 2000. – V. 60. – № 24. – P.6958–6963.371. Yuan H. Synthesis of Anti-Angiogenic Isocoumarins / H. Yuan, B.

Junker, P. Helquist, R.E. Taylor // Curr. Org. Synth. – 2004. – V. 1. – № 1. – P. 1–9.372. Ichinose K. 2-(8-Hydroxy-6-methoxy-1-oxo-1H-2-benzopyran-3-yl)propionic acid, an inhibitor of angiogenesis, ameliorates renal alterations in obese type 2 diabetic mice / K.Ichinose, Y. Maeshima, Y. Yamamoto, M.

Kinomura, K. Hirokoshi, H. Kitayama, Y.Takazawa, H. Sugiyama, Y. Yamasaki, N. Agata, H. Makino // Diabetes – 2006. – V. 55. –№ 5. – 1232–1242.373. Ichihara A. Structure, Synthesis and Stereochemistry of (+)-Orthosporin, a Phytotoxic Metabolite of Rhynchosporium Orthosporum / A. Ichihara, M. Hashimoto, T. Hirai, I. Takeda,Y. Sasamura, S. Sakamura, R. Sato, A. Tajimi // Chem. Lett. – 1989. – V. 18. – № 8. – P.1495–1498.374. Kerrigan, J.

E. Mechanism-Based Isocoumarin Inhibitors for Human Leukocyte Elastase.Effect of the 7-Amino Substituent and 3-Alkoxy Group in 3-Alkoxy-7-amino-4-chloroisocoumarins on Inhibitory Potency / J. E. Kerrigan, J. Oleksyszyn, C.-M. Kam, J. Selzler, J.C. Powers // J. Med. Chem. – 1995. – V. 38. – № 3. – P. 544–552.375. Hallock Y. F. De-O-methyldiaporthin, a phytotoxin from Drechslera siccans / Y. F.Hallock, J. Clardy, D. S.

Kenfield, G. Strobel // Phytochemistry – 1988. – V. 27. – № 10. –P. 3123–3125.376. Arnone A. Cryphonectric acid and other minor metabolites from a hypovirulent strain ofCryptonectria parasitica / A. Arnone, G. Assante, G. Nasini, S. Strada, A. Vercesi // J.Nat. Prod. – 2002. – V. 65. – № 1. – P. 48–50.376377. Costa P. R.

R. Vanillin as starting material for the synthesis of isomeric phthalides / P. R.R. Costa, C. C. Lopes, R. S. C. Lopes, M. F. G. Marinho, R. N. Castro // Synth. Commun. –1988. – V. 18. – № 14. – P. 1723–1730.378. Starling S. M. Synthesis of 2-substituted furanonaphthoquinones using directed metalationand cross coupling reactions / S.

M. Starting, D. S. Raslan, A. B. de Oliveira // Synth.Commun. – 1998. – V. 28. – № 6. – P. 1013–1030.379. Дмитриев А. С. Новый синтез 3-(2-фурил)фталидов / А. С. Дмитриев, А. С. Пилипенко, В. Т. Абаев, А. В. Бутин // ХГС – 2005. – № 9. – c. 1302–1304.380. Butin A. V.

Synthesis and some transformations of new 9-furylnaphtho[2,3-b]furan derivatives / A. V. Butin, V. V. Mel’chin, V. T. Abaev, W. Bender, A. S. Pilipenko, G. D. Krapivin // Tetrahedron – 2006. – V. 62. – № 34. – P. 8045–8053.381. Mel’chin V. V. Furan ring opening – furan ring closure: cascade rearrangement of novel 4acetoxy-9-furylnaphtho[2,3-b]furans / V. V. Mel’chin, A. V. Butin // Tetrahedron Lett.

–2006. – V. 47. – № 25. – P. 4117–4120.382. Pandarus V. A New Class of Heterogeneous Platinum Catalysts for the ChemoselectiveHydrogenation of Nitroarenes / V. Pandarus, R. Ciriminna, F. Beland, M. Pagliaro // Adv.Synth. Catal. – 2011. – V. 353. – № 8. – P. 1306–1316.383. Hirano K. A Modular Synthesis of Highly Substituted Imidazolium Salts / K. Hirano, S.Urban, C.

Wang, F. Glorius // Org. Lett. – 2009. – V. 11. – № 4. – P. 1019–1022.384. Bennour S. General acid-catalyzed addition of methanol to (E)-N-benzylideneanilines / S.Bennour, J. Toullec // Can. J. Chem. – 1999. – V. 77. – № 5–6. – P. 760–773.385. Erbea R. -Thioamidoalkylating Agents; Preparation of N-(-Alkoxyalkyl)-thioamidesfrom Thioamides and Acetals / R. Erbea, S. Panossian, C.

Giordano // Synthesis – 1977. –№ 4. – P. 250–252.386. Breuer S. W. N-Benzoylbenzaldimines and N--Alkoxybenzylbenzamides / S. W. Breuer,T. Bernath, D. Ben-Ishai // Tetrahedron – 1967. – V. 23. – № 6. – P. 2869–2877.387. Kumar S. Synthesis of cytotoxic and antioxidant Schiff’s base analogs of aloin / S. Kumar,D. P. Matharasi, S. Gopi, S. Sivakumar, S. Narasimhan // J. Asian Nat. Prod. Res. – 2010.– V. 12.

– № 5. – P. 360–370.388. Kuo Y.-H. A New Method for Preparation of 3-Hydroxypyridines from Furfurylamines byPhotooxygenation / Y.-H. Kuo, K.-S. Shih // Chem. Pharm. Bull. – 1991. – V. 39. – № 1. –P. 181–183.389. Sarang P. S. Synthesis of Advanced Intermediates of Lennoxamine Analogues / P. S. Sarang, A. A. Yadav, P. S. Patil, U. M.

Krishna, G. K. Trivedi, M. M. Salunkhe // Synthesis –2007. – № 7. – P. 1091–1095.377390. Bhowmik S. Expeditious synthesis of chiral 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazines / S.Bhowmik, A. K. S. Kumar, S. Batra // Tetrahedron Lett. – 2013. – V. 54. – № 18. – P.2251–2254.391. Stetter H. Herstellung bi- und tricyclischer Pyrrol-Systeme / H. Stetter, P.

Lappe // LiebigsAnn. Chem. – 1980. – № 5. – S. 703–714.392. Thurston D. E. Synthesis of DNA-Interactive Pyrrolo[2,1-c][1,4]benzodiazepines / D. E.Thurston, D. S. Bose // Chem. Rev. – 1994. – V. 94. – № 2. – P. 433–465.393. Corelli F. Heterocyclic systems. 5. Synthesis and activity on the CNS of derivatives of 6Hpyrrolo[1,2-a][1,4]benzodiazepine / F. Corelli, S. Massa, G. C. Pantaleoni, G.

Palumbo, D.Fanini // Farmaco – 1984. – V. 39. – № 8. – P. 707–717.394. Mai A. Pyrrolobenzodiazepines with antinociceptive activity – synthesis and pharmacological activities / A. Mai, R. Di Santo, S. Massa, M. Artico, G. C. Pantaleoni, R. Giorgi, M.F. Coppolino, A.