Синтез пиррольных интермедиатов для высокосопряженных порфиринов
Рефераты >> Химия >> Синтез пиррольных интермедиатов для высокосопряженных порфиринов

[29] Rigo B., Valligny D., Taisne S., Couturier D. Disilylated compounds as precursors of heterocycles. //J.Synth.Commun. 1988 v.18 p.170-171.

[30] Hendrickson J.B., Ress R.W., Templeton J.F. General heterocycle synthesis. Use of acetyl‑enedicarboxylic esters. //J.Am.Chem.Soc. 1964 v.86 p.107-111.

[31] Grob C.A., Schacl H.P. Eine nene pyrroling- synthese II. Teil untersuchungen inder pyrrolreihe. //Helv.Chim.Acta 1955 v.38 p.1121-1127.

[32] Spence J.D. and Lash T.D. Porphyrins with exocyclic rings. Part 14. Synthesis of tetraacenaphthoporphyrins, a new family of highly conjugated porphyrins with record‑breaking long‑ wavelengh electronic absorptions. //J.Org.Chem. 2000 v.65 p.1530-1539.

[33] Bastian J.A. and Lash T.D. Porphyrins with exocyclic rings. Part 12. Synthesis of meso, b‑butano- and meso, b‑pentanoporphyrins from cycloalka[b]pyrrole. //Tetrahedron 1998 v.54 p.6299-6310.

[34] Gotthardt H., Huisgen R. And Bayer H.O. 1.3-Dipolar cycloaddition reactions. L III. The question of the 1.3-dipolar nature of 2-oxazolin-5-ones. //J.Am.Chem.Soc. 1970 v.92 p.4340‑4343.

[35] Arcadi A. and Rossi E. Synthesis of functionalised furans and pyrroles through annulation reactions of 4-pentynones. //Tetrahedron 1998 v.54 p.15253-15272.

[36] Sessler J.L., Davis J.M., Lynch V. Synthesis and characterization of a stable smaragdyrin isomer. //J.Org.Chem. 1998 v.63 p.7062-7065.

[37] Alberola A., Ortega A.G., et.al. Versatility of Weinreb amides in the Knorr pyrrole synthesis. //Tetrahedron 1999 v.55 p.6555-6566.

[38] Hombrecher H.K., Horter G. Synthesis of pyrroles via ethyl N- (3‑oxo‑1‑alkenyl) glycinates. //Synthesis 1990 p.389-391.

[39] Ferraz H.M.C., Oliveira E.O., et.al. A new and efficient approach to cyclic b‑enamino esters and b‑enamino ketones by iodine- promoted cyclization. //J.Org.Chem. 1995 v.60 p.7357-7359.

[40] Ferraz H.M.C., Pereira F.L.C., et.al. Synthesis of N‑substituted pyrrole and tetrahydroindole derivatives from alkenyl b‑dicarbonyl compounds. //Tetrahedron 1999 v.55 p.10915‑10924.

[41] Рындина С.А., Кадушкин А.В., Соловьева Н.П., Граник В.Г. Циклизация Торпа‑ Циглера в синтезе 3‑ амино‑ 4‑ цианопиррола. //ХГС 2000 т.26 с.1643-1655.

[42] Chen N., Lu Y., Gadamasetti K., et.al. A short, facile synthesis of 5-substituted 3‑amino‑1H‑pyrrole‑2‑carboxylates. //J.Org.Chem. 2000 v.65 p.2603-2605.

[43] Порфирины: структура, свойства, синтез. // Под ред. Ениколопяна Н.С. М.: Наука, 1985. 333с.

[44] Rose E., Soleihavoup M., et al. Bis-faced aminoporphyrin templates for the synthesis of chiral catalysts and hemeprotein analogues. // J.Org.Chem. 1998 v.63 №6 p.2042-2044.

[45] Ono N., Muratani E., et al. Synthesis of 2,7,12,17‑tetraaryl-3,8,13,18-tetranitroporphyrins; electronic effects on aggregations of porphyrins. // J.Chem.Soc., Perkin Trans.1 1998 №22 p.3819-3824.

[46] Tse M.K., Zhou Z., et al. Regioselective bromination and subsequent suzuki cross-coupling of highly electron deficient 5,10,15,20-tetrakis(trifluoromethyl)porphyrin. // Tetrahedron 2000 v.56 p.7779-7783.

[47] Czuchajonski L., Habdas J., et al. Porphyrinyl-uridines as the first water soluble porphyrinyl-nucleosides. // Tetrahedron Letters 1991 v.32 p.7511-7514.

[48] Shin J.-Y., Minezawa N., et al. Study for expanded porphyrins producted during the condensation reaction of pentafluorobenzaldehyde and pyrrole. // Abstracts of ICPP-1, Dijon, France, 2000, post 562.

[49] Ono N. A new synthesis of highly conjugated porphyrins. // Abstracts of ICPP-1, Dijon, France, 2000, sym 147.

[50] Ono N., Hironaga H., et al. A new synthesis of pyrroles and porphyrins fused with aromatic rings. // J.Chem.Soc., Perkin Trans.1 1996 p.417-423.

[51] Nguyen L.T., Senge M.O., Smith K.M. One-pot synthesis of regiochemically pure porphyrins from two different pyrroles. // Tetrahedron Letters 1994 v.35 p.7581-7584.

[52] Nguyen L.T., Senge M.O., Smith K.M. Simple methology for syntheses of porphyrins possessing multiple peripheral substituents with an element of symmetry. // J.Org.Chem. 1996 v.61 p.998-1003.

[53] Березин Б.Д. // Координационные соединения порфиринов и фталоцианина / М.: Наука 1978 150с.

[54] Arsenault G.P., Bullock E., MacDonald S.F. Pyrromethanes and porphyrins there from. // J.Am.Chem.Soc. 1960 v.82 p.4384-4387.

[55] Clarke O.J., Boyle R.W. Selective synthesis of asymmetrically substituted 5,15‑diphenylporphyrins. // Tetrahedron Letters 1998 v.39 p.7167-7168.

[56] Lee C.-H., Li F., Iwamoto K., Lindsey J.S. Synthetic approaches to regioisomerically pure porphyrins bearing four different meso-substituents. // Tetrahedron 1995 v.51 p.11645-11654.

[57] Balasubramanian T., Lindsey J.S. synthesis of b-substituted porphyrin building blocks and conversion to diphenylethyne-linked porphyrin dimers. // Tetrahedron 1999 v.55 p.6771‑6784.

[58] Maruyama K., Nagata T., Ono N., Osuka A. A synthesis of unsymmetric porphyrin dimers // Bull.Chem. Soc.Jpn. 1989 v.62 p.3167-3170.

[59] Ema T., Kuroda Y., Ogoshi H. Selective syntheses of unsymmetrical meso-arylporphyrins. // Tetrahedron Letters 1991 v.32 p.4529-4532.

[60] Wallaca D.M., Leung S.H., Senge M.O., Smith K.M. Rational tetraarylporphyrin syntheses: tetararylporphyrins from the MacDonald route. // J.Org.Chem. 1993 v.58 p.7245-7257.

[61] Мамардашвили Н.Ж., Голубчиков О.А. Синтез порфиринов из дипирролилметанов. // Успехи химии 2000 т.69 с.342-354.

[62] Scog W.R., Yong H.N., Youngkyu D. Synthesis, structures and electrchemical characterization of ferrocene-substituted porphyrin and porphodimethene. // Inorg.Chim.Acta 2000 v.309 p.49-56.

[63] Tjahjono D.H., Akutsu T., et al. Cationic porphyrins bearing diazolium rings: synthesis and their interaction with calf thymus DNA. // Biochimica et Biophysica Acta/General Subjects 1999 v 1472 p.333-343.

[64] Smith K.M., Craig J., Medforth D.T.L. Syntheses, stability and tumorcidal activity of porphyrin dimers and trimers with ether linkages. // Tetrahedron Letters 1990 v.31 p.7265-7270.

[65] Khoury R.G., jaquinod L., Smith K.M. Metal ion-induced self assembly of open-chain tetrapyrrole derivatives: double stranded dinuclear complexes from 10-oxo-5,15-biladienes. // Tetrahedron 1998 v.54 p.2339-2346.

[66] Dolphin D.M., Johnson A.W., Long J. Porphyrinogens and porphodimethenes, intermediates in the synthesis of meso-tetraphenylporphyrins from pyrroles and benzaldehyde. // J.Heterocycl.Chem. 1970 v.7 p.275-283.

[67] Smith K.M., Minnetian O.M. Anomalous cyclization of 1,19-dimethyl-a,c-dimethyl-a,c-biladiens: direct synthesis of meso-aminoporphyrin derivatives. // Synth.Commun. 1985 v.15 p.75-80.

[68] Smith K.M., Minnetian O.M. Cyclization of 1’,8’-dimethyl-a,c-biladiene salts to give porphyrins: a study with various oxidizing agents. // J.Chem.Soc.,Perkin Trans.1 1986 p.277‑280.


Страница: