Dr. Schneider Gyula KÖNYVEK, KÖNYVFEJEZETEK 1. A papírkromatográfia kézikönyve Kovács, Ö., Schneider Gy. Akadémiai Kiadó, Budapest 1961. p.850 (Hais, I., Macek, K. Handbuch der Papierchromatographie, Ed by VEB Gustav Fischer Verlag, Jena 1958. Fordítás, szerkesztés és lektorálás) 2. Rearrangements of alcohols, phenols, diols and peroxides Schneider, Gy. (In: The chemistry of functional groups Suppl. E: The chemistry of hydroxyl, ether and peroxide groups, Vol. 2. Ed. By S. Patai. Chichester, 1993. J. Wiley and Sons Ltd. Chapter 14, 785-841. p.) 3.
Epoxidation of C=X double bonds Bartók, M., Schneider, Gy. (In: The chemistry of functional groups Suppl. A3: The chemistry of double-bonded functional groups. Ed. By S. Patai. Chichester, 1997. J. Wiley and Sons Ltd. Chapter 20, 1223-1251.p.)
SZABADALMAK 1.
Eljárás új, szteroid-16-(5’-spiro-1’,3’–dioxanil) vegyületek előállítására. Schneider Gy., Weisz I.-né, Polák A., Vass A., Dömök I.-né, Mészáros Cs., Szporny L.: Ger. Offen, 2.547.840 (C.A. 85, 46947, 1976).
2.
Eljárás új, helyettesített szteroid-16-(5’-spiro-1’,3’-dioxanil) vegyületek előállítására Schneider Gy., Weisz I.-né, Polák A., Vass, A., Dömök I.-né, Mészáros Cs., Szporny L.: Ger. Offen, 2.547.841 (C.A. 85, 63244, 1976).
3.
Eljárás új, 16-(5’-spiro-1’,3’-dioxanil)-szteroidok előállítására. Schneider Gy., Weisz I.-né, Polák A., Vass A., Dömök I.-né, Mészáros Cs., Szporny L.: Ger. Offen, 2.547.842 (C.A. 85, 46946, 1976).
4.
Novel 17β-hydroxysteroid dehydrogenase type I inhibitors. Solvay Pharmaceuticals GmbH. Hannover (Germany). p: 1-198. Messinger J., Thole H. H., Bettina H., Van Steen, J.B., Schneider, Gy., Hulshof J. B. E., Koskimies, P., Johansson, N., Adamski, J. International Publication Number: WO 2005/047303 A2
REFERÁLT TUDOMÁNYOS CIKKEK 1.
Isolierung und Reindarstellung der Aristolochiasäure Schneider, Gy., Szőke, J., Kovács, S. Arch. Exp. Path. und Pharmak. 1958, 234, 566-567.
2.
Investigation on yeasts producing red pigments. I. Effect of diphenylamine on the carotenoids produced by yeasts. Schneider, Gy., Matkovics., Zsolt, J. Acta Phys. et Chem., Szeged 1959, 5, 55-58.
3.
Effect of diphenylamine on the synthesis of carotene Schneider, Gy., Matkovics, B., Zsolt, J., Kovács, Ö. Nature 1960, 186, 235.
4.
Isolation of aristolochic acid from Aristolochia Clematitis native in Hungary. The preparation of physiologically active aristolochia derivatives Schneider, Gy. Acta Phys. et Chem. Szeged 1960, 6, 92-96.
5.
Néhány adat a difenilamin karotinoid szintézisére gyakorolt hatására vonatkozóan Schneider, Gy., Matkovics B., Zsolt, J. MTA Biol. Csoport Közleménye 1960, 4, 281-285.
6.
Cis- and trans-7-oxabicyclo-[4.2.0]-octane Kovács, Ö., Tuba, Z., Weisz, I., Schneider, Gy. Chem. and Ind. 1961, 1222.
7.
Himija okiszi trimetilene. Szoobscsenie 1. Cisz- i transz-7-okszabiciclo-[4.2.0]-oktan. Kovács, Ö., Tuba, Z., Weisz, I., Schneider, Gy. Izveszt. Akad. Nauk SzSzSzR, Otdel. Him. Nauk. 1962, 130-138.
8.
Trimetilén-oxid szármzékok kémiája, I. Cisz- és transz-7-oxabiciklo-[4.2.0.]-oktán. Kovács, Ö., Tuba, Z., Weisz, I., Schneider, Gy. Magyar Kémiai Folyóírat 1963, 69,37-41.
9.
Carotenoid changes in different maiz varieties during repening Zsolt, J., Schneider, Gy., Matkovics B. Canad. J. Biochem. Physiol. 1963, 41, 481-486.
10. Über die Herstellung einiger am Stickstoffatom substituierter 1,3-Propandiol-dicarbamate Schneider, Gy., Halmos, M., Mészáros, P., Kovács, Ö. Monatshefte für Chemie 1963, 94, 426-433.
11. Solvolysis of 2-hydroxymethylcyclohexanol derivatives Kovács, Ö., Schneider, Gy., L.Láng, K. Proc. Chem. Soc. 1963, 374. 12. Mechanizme izomerizacii v ψ-tropin Kovács, Ö., Schneider, Gy., Uresch, F. Izeszt. Akad. Nauk SzSzSzR. Szerija Him. 1964, 320-326. 13. Synthesis of m-dioxanes Schneider, Gy., Kovács, Ö., Chinorai, M. Acta Phys. et Chem. Szeged 1964, 10, 95-104. 14. Trimetilén-oxid származékok kémiája, III. Cisz-6-oxabiciklo-[3.2.0.]-heptán Kovács, Ö., Szilágyi, J., Schneider, Gy. Magyar Kémiai Folyóírat 1965, 71, 93-98. 15. Synthesis of 2-methyl-cis-4,5-tetramethylene-1,3-dioxenium tetrafluoroborate Schneider, Gy., Kovács, Ö.K.J. Chem. Commun.. 1965, 202-203. 16. Synthesis of substituted 1,3-dioxenium salts Schneider, Gy. Tetrahedron Letters 1966, 5921-5923. 17. Neighbouring group participation I. (AcO-6) participation in the solvolysis of 2-hydroxymethyl cyclohexanol derivatives Kovács, Ö.J.K., Schneider, Gy., L. Láng, K., Apjok, J. Tetrahedron 1967, 23, 4181-4196. 18. Neighbouring benzoyl group participation in 1,2- and 1,3-diol system Schneider, Gy., L.Láng, K. Chem. Commun. 1967, 13-14. 19. Neighbouring group participation in 17-hydroxy-16-hydroxymethyl steroids Schneider, Gy., Weisz-Vincze, I. Chem. Commun. 1968, 1030-1031. 20. Alfa-gamma diszubsztitutált szteroidok térszerkezetének vizsgálata Schneider, Gy., Weiszné Vincze I. Kémiai Közlemények 1969, 31, 383-397. 21. The effect of spectrl composition of the light on the chlorophyll and carotenoid contents of bean leaves (Phaseolus vulgaris, L.) Szalay, L., Tombácz, E., Bálint, E., Horváth, I., Schneider, Gy. Acta Biol. Szeged 1969, 15, 51-56.
22. Steroids. XIII. 16-Substituted steroids Weisz- Vincze, I., Schneider, Gy., Halmos, M., Szabó J.A., Kovács, K. Acta Phys. et Chem. Szeged 1971, 17, 67-84. 23. Ring expansion of steroid oxetanes to acetals Schneider, Gy., Weisz-Vincze, I., Vass, A., Kovács, K. Chem. Commun. 1972, 713. 24. Stereoselective deacetylation and stereospecific acyl migration of steroid acetates on aluminium oxide Schneider, Gy., Weisz-Vincze, I., Vass, A., Kovács, K. Tetrahedron Letters 1972, 3349-3352. 25.
13
C-FT-NMR-Untersuchungen an Steroide. Konfigurationszuordnung an 16,17-Disubstituierten ∆-1,3,5(10)-östratrienen und ∆ -5(6)-Androstenen Engelhardt, G., Schneider, Gy., Weisz-Vincze, I., Vass, A. J. prakt. Chem. 1974, 316, 391-401.
26. Front side neighbouring group participation in 16-hydroxymethyl17-hydroxysteroids Schneider, Gy., Weisz-Vincze, I. Tetrahedron Letters 1975, 2115-2118. 27. p-Toluolszulfonsavészterek oxidációjakor fellépő szomszédcsoport részvétel Schneider, Gy., Weiszné Vincze I., Kémiai Közlemények 1975, 44, 427-435. 28. Szteroidok FT-CMR spetrumának teljes hozzárendelése, a konfiguráció és a CMR-kémiai eltolódások közötti összefüggések vizsgálata Schneider, Gy., Weiszné Vincze I., Engelhardt, G. Kémiai Közlemények 1976, 46, 365-374. 29. Antibacterial effect, plasmid curing activity and chemical structure of some tricyclic compounds Molnár, J., Mándi Y., Holland, I.B., Schneider, Gy. Acta Microbiol. Acad. Sci. Hung. 1977, 24, 1-6. 30. Steroide, LIII. 1-NMR-Untersuchungen. Konfigurationszuordnung von 16-substituiertrn 17-Hydroxy-Steroiden Schönecker, B., Trasselt, D., Draffen, J., Ponsold, K., Engelhardt, G., Zeigan, D., Schneider, Gy., Weisz-Vincze, I. J. prakt. Chem 1977, 319, 419-431. 31. Ritter-Reaktionen an Steroiden, I. Öffnung der epimeren 16,17-Epoxide des 3-Methoxy-östra-1,3,5(10)-triens mit Nitrilen Schneider, Gy., Schönecker, B. Acta Chim. Acad. Sci. Hung. 1977, 95, 321-331.
32. Antibacterial and plasmid-curing effect of some tricyclic comounds on Escheria coli K12 F,lac. Molnár, J., Mándi, Y., Holland, I.B., Schneider, Gy. Acta Microbiol. Acad. Sci. Hung. 1977, 24, 83-89. 33. Steroids, XIX. Neighbouring group participation, III. (AcO-6) and PrO-6) neighbouring group participation in the 16-hydroxymethylandrost-5-ene3,17-diol series Schneider, Gy., Vincze, I., Vass, A. Acta Chim. Acad. Sci. Hung. 1979, 99, 51-67. 34. Ujabb eredmények a gyógyászatilag hatásásos szteroidok kutatásában Schneider, Gy. Magyar Kémikusok Lapja 1980, 35, 148-156. 35. New synthesis of steroidal tetrahydro-oxazin-2-ones Schneider, Gy., Hackler, L., Dombi, Gy. J. C. S., Chem. Commun. 1980, 891-892. 36. Ring expansion of steroid oxethanes into dihydrooxazines Schneider, Gy., Hackler, L., Sohár, P. Tetrahedron letters 1981, 22, 341-344. 37. Stereoselective reduction of a hydroxymethylene keto steroide Vincze, I., Somlai, Cs., Schneider, Gy., Dombi, Gy. Acta Chim. Acad. Sci. Hung. 1980, 106, 359-361. 38. Steroids, XXVII. Neighbouring group participation, IV. Preparation of 16α-Hydroxymethyandrost-5-ene-3β,17α-diol Schneider, Gy., Vincze, I., Vass, A., Hackler, L., Dombi, Gy. Acta Chim. Acad. Sci. Hung. 1982, 109, 71-82. 39. Steroids, XXVIII. Neighbouring group participation, V. (O—-4) Neighbouring group participation and fragmentation int he 16-hydroxymethylandrost-5-ene-3,17-dol series Schneider, Gy., Vincze, I., Hackler, L., Szabó J.A., Dombi, Gy. Acta Chim. Acad. Sci. Hung. 1982, 110, 429-440. 40. Ritter- reaktionen an Steriden, II. Reaktion der Epimeren 14,15-Epoxide und des 15β,16β-Epoxids der Östratrien-Reihe mit Acetonitril und BF3–Etherat Schubert, G., Schneider, Gy., Schade, W., Dombi, Gy. Acta Chim. Acad. Sci. Hung. 1982, 111, 173-187. 41. Steroids, XXIX. Neighbouring group participation, VI. N-aryalurethane neighbouring group participation in the 16-hydroxymethylandrost-5ene-3,17-diol series Schneider, Gy., Hackler, L., Sohár, P. Acta Chim. Acad. Sci. Hung. 1982, 111, 285-296.
42. Front side neighbouring group participation in the 16-hydroxymethylandrost-5-ene-3,17-diol series Schneider, Gy., Vincze, I., Domb, Gy. Tetrahedron 1982, 38, 2729-2732. 43. Convenient method for the formation of 16-methylene-17-ketosteroids Schneider, Gy., Vincze, I., Hackler, L., Dombi, Gy. Synthesis 1983, 665-669. 44. Configurational analysis of 16-methyl-androstene-5 deriatives Schneider, Gy., Meskó, E., Hackler, L., Dombi, Gy., Zeigan, D., Engelhardt, G. Tetrahedron 1984, 40, 1205-1211. 45. A Convenient Method for the Preparation of 16,16-Bishydroxymethyl-17hydroxysteroids and 16,16-Bishydroxymethyl-17-oxosteroids Schneider, Gy., Wölfling, J., Hackler, L., Meskó, E., Dombi, Gy. Synthesis 1985, 194-197. 46. Steroids. Part 32. Configurational analysis of 16-methyltestosterone derivatives Schneider, Gy., Meskó, E., Hackler, L., Dombi, Gy., Zeigan, D., Engelhardt, G. J. Chem. Soc. Perkin Trans. 1 1985, 1597-1600. 47. Ritter-reaction on steroids. Ring expansion of steroid oxethans into dihydrooxyzines Schneider, Gy., Hackler, L., Sohár, P. Tetrahedron 1985, 41, 3377-3386. 48. Steroids. Part. 34. Configurational Analysisi of 3-Hydroxy-2-methyl5α-cholestane Derivatives Schneider, Gy., Meskó, E., Dombi, Gy., Zeigan, D., Engelhardt, G. J. Chem. Research (S), 1987, 12-13. J. Chem. Research (M) 1987, 201-214. 49. 2-(Hydroxymethyl)androstene Derivatives Vincze, I., Somlai, Cs., Schneider, Gy., Dombi, Gy., Kálmán, A. Liebigs Ann. Cem. 1987, 499-504. 50. New synthesis of Steroidal Tetrahydrooxazin-2-ones Schneider, Gy., Hackler, L., Sohár, P. Tetrahedron 1987, 43, 3987-3995. 51. Hidroximetilezett szteroidok és származékaik Schneider, Gy., Vincze I. Gyógyszerészeti Tudomány Aktuális Kérdései 1987, 2, 85-140. 52. Steroids 35. Synthesis of 16,16-Dimethyl-17β-hydroxysteroids. Schneider, Gy., Wölfling, J., Meskó, E., Dombi, Gy. Steroids 1988, 51, 317-327.
53. Steroids 36. Synthesis of 16,16-Dimethyl-17-ketosteroids and 16,16-Dimethyl-17βhydroxysteroids Wölfling, J., Schneider, Gy., Dombi, Gy. Steroids 1988, 51, 329-335. 54. Steroids, XXXVII., Neighbouring Group Participation, VIII. Neighbouring Group Participation in the 16-Hydroxymethyl-3-methoxyestra-1,3,5(10)-trien-17β-ol Series Schneider, Gy., Vass, A., Vincze, i., Sohár, P. Liebigs Ann. Chem. 1988, 267-273. 55. Steroids, XXXVIII., Neighbouring Group participation, IX. Preparation of 16α-Hydroxymethyl-3-methoxyestra-1,3,5(10)-trien-17α-ol and Solvolysis Investigations Schneider, Gy., Hackler, L., Sohár, P. Liebigs Ann. Chem. 1988, 679-683. 56. 15-(Hydroxymethyl)androstene and –estratriene Derivatives. Steroids, XL. Vincze, I., Somlai, Cs., Schneider, Gy., Dombi, Gy. Liebigs Ann. Chem. 1988, 973-978. 57. Structure of a D-Homoestrone Derivative Antel, J., Sheldrick, G.M., Tietze, L.-F., Wölfling, J. Acta Crystallographica 1988, C 44, 2229-2230. 58. Neighbouring Group Participation and Fragmentation During the Solvolysis of the Epimers of 3-Methoxy-16-(tolyl-sulfonyloxymethyl)-estra-1,3,5(10)-trien-17-ol Schneider, Gy., Bottka, S., Hackler, L., Wölfling, J., Sohár, P. Liebigs Annalen für Chemie 1989, 263-267. 59. Steroids, XLII., Configurational Analysis of 3-Methoxy-16-methylestra1,3,5(10)-trien-17-ol Derivatives Meskó, E., Schneider, Gy., Dombi, Gy., Zeigan, D. Liebigs Ann. Chem., 1990, 419-422. 60. Steroids. Part 43. Thermal Decomposition of Steroidal Azidoformates Schneider, Gy., Hackler, l., Szanyi, J., Sohár, P. J. Che. Soc. Perkin Trans. 1 1991, 37-42. 61. Seroids, XLIV., Neighbouring Group Participation, XI. Decomposition of 2-Amidomethylene-3-hydroxysteroids Vincze, I., Somlai, Cs., Schneider, Gy. Liebigs Ann. Chem. 1991, 1049-1052. 62. Inter- and Intamolecular Hetero Diels-Alder reactions, 31. Synthesis of D-Homoestrone Derivatives by Tandem Knoevenagel Hetero DielsAlder Reactions from Natural Estrone Tietze, L.-F., Wölfling, J., Schneider, Gy. Chemische Berichte 1991, 124, 591-594.
63. Binding of Glucocorticoid Analoges to Human Placental Glucocorticoid Receptors Halmos, G., Schneider, Gy., Falkay, Gy. Proc. Of the 4th Symposium on the Analysis of Steroids. Pécs, Hungary. 1990. (Görög, S., ed.) Akadémiai Kiadó, Budapest 1991 p. 37-41. 64. Steroids, XLV., Neghbouring group participation, XII. Decomposition of (Z)-16-Aminomethylene-17β-hydroxysteroids Mediated by Neighbouring group participation Vincze, I., Somlai, Cs., Schneider, Gy., Dombi, Gy. Lebigs Ann. Chem. 1992, 187-192. 65. Steroids, L., Ring D Cleveage of D-Trisubstiteted Steroids Vincze, I., Somlai, Cs., Schneider, Gy. Liebigs Ann. Chem. 1992, 1103-1107. 66. N-Arylurethane Neighbouring Group Participation during Solvolysis of 3-Methoxy-17-N-phenylcarbamoyloxy-16-p-tolylsulfonyloxymethylestra1,3,5(10)-triene Streoisomers Hackler, l., Schneider, Gy., Sohár, P. Tetrahedron 1992, 48, 9305-9314. 67. Az ivari szagért felelős androsztenon elleni aktív immunizáció kan sertésekben II. Immunizáció testidegen androsztenonszármazékokból előállított antigénekkel Házas, Z., Horn, P., Fehér, T., Sándor E., Hackler, L., Schneider, Gy. Magyar Állatorvosok Lapja 1992, 47, 590-596. 68. Stereoselective Synthesis and Determination of the C-16 Configuration of 16Halomethyl/16-Hydroxymethyl Steroids Sohár, P., Fürjes, A., Wölfling, J., Schneider, Gy. Synthesis 1992, 1280-1283. 69. Configurational Analysis of 16-Methyl-19-nor-testosterone Derivatives Meskó, E., Dombi, Gy., Lukács, ., Schneider, Gy. Liebigs Ann. Chem. 1993, 923-925. 70. Synthesis of New 16-Spirosteroids Tietze, L. F., Wölfling, J., Schneider, Gy., Noltemeyer, M. Steroids 1994, 59, 305-309. 71. In vitro Inhibitory Effects of 16-Methyl-substituted Steroids on 5a-Reductase in Rat and Human Prostate Faredin, I., Tóth, I., Wölfling, J., Schneider, Gy., Meskó, E. Steroids, 1994, 59, 568-571. 72. A D-Homotestosterone Derivative Noltemeyer, M., Tietze, L. F., .Wölfling, J, Schneider, Gy. Acta Crystallographica, 1994, C50, 726-727.
73. 3-Methoxy-16,16-dimethyl-5α-androstan-17-one Wölfling, J., Schneider, Gy., Noltemeyer, M., Tietze, L. F. Acta Crystallographica, 1994, C50, 964-965. 74. 16-Metil-szubsztituált szteroidok in vitro gátló hatása az 5α-reduktáz aktivitására patkány és emberi prosztatában Faredin, I., Tóth, I., Wölfling, J., Schneider, Gy., Meskó, E.: Acta Pharmaceutica Hungarica 1994, 64, 171-174. 75. Carbon-13 NMR data for methylated steroids Meskó, E., Schneider, Gy., Dombi, Gy., Zeigan, D. Magn. Reson. Chem. 1994, 32, 565-567. 76. In Vitro Binding of 16-Methylated C18 and C19 Steroid Derivatives to the Androgen Receptor Tóth, I., Faredin, I., Meskó, E., Wölfling, J., Schneider, Gy., Pharmacological Research 1995, 32, 217-221. 77. The Ursodeoxycholic Acid - p-Aminobenzoic Acid Loading Test, a New Diagnostic Tool in the Bacterial Overgrowth Syndrome Kiss, Zs. F., Wölfling, J., Csáti, S., Nagy, F., Wittmann, T., Schneider, Gy., Lonovics, J. Z. Gastroenterol. 1995, 33, 295. 78. A Fluorinated D-Homoestrone Derivative Noltemeyer, M., Tietze, L. F., .Wölfling, J., Frank, É., Schneider, Gy. Acta Crystallographica, 1996, C52, 2258-2259. 79. Steroids 54. Amino acylaminosteroids Vincze, I., Hackler, L., Szendi, Zs., Schneider, Gy. Steroids 1996, 61, 697-702. 80. The Ursodeoxycholic Acid Loading Test, a New Diagnostic Tool in the Bacterial Overgrowth Syndrome Kiss, Zs. F., Wölfling, J., Csáti, S., Nagy, F., Wittmann, T., Schneider, Gy., Lonovics, J. Gut, 1996, 39, Suppl. No. 3, A173. 81. Az urzodezoxikólsav-p-aminobenzoesav teszt a kontaminált vékonybélszindróma diagnosztikájában F. Kiss, Zs., Wölfling, J., Csáti, S., Nagy, F., Lonovics, J., Schneider, Gy. Orvosi Hetilap 1997, 138, 1255-1258. 82. The ursodeoxycholic acid-p-aminobenzoic acid deconjugation test, a new tool for the diagnosis of bacterial overgrowth syndrome F.Kiss, Zs., Wölfling, J., Csáti, S., Nagy, F., Wittmann, T., Schneider, Gy., Lonovics, J. European Journal of Gastroenterology and Hepatology 1997, 9, 679-682.
83. A Steroidal Dihydro-1,3-oxazine Derivative Bes, T., Hajnal, A., Schneider, Gy., Noltemeyer, M., Wölfling, J. Acta Cryst. 1998, C54, 372-373. 84. Homogenous and Heterogenous Asymmetric Reactions. Part IX. Asymmetric Transfer Hydrogenation of 16-Methyl-substituted steroid 17-ketones in the Presence of Rhodium(I) complexes Török, B., Wölfling, J., Schneider, Gy., Bartók, M., React. Kinet. Catal. Lett. 1998, 64, 35. 85. One-step conversion of oxetane-fused to 1,3-oxazine-fused steroids Hajnal, A., Wölfling, J., Schneider, Gy., Collect. Czech. Chem. Commun. 1998, 63, 1613-1622. 86. Efficient Synthesis of a Novel Estrone-Talaromycin Hybrid Natural Product Tietze, L. F., Schneider, Gy., Wölfling, J., Nöbel, T., Wulff, C., Schubert, I., Rübeling, A. Angew. Chem. 1998, 110, 2644-2646. Angew. Chem. Int. Ed. 1998, 37, 2469-2470. 87. A Hexacyclic Estrone Derivative Bes, M. T., Wölfling, J., Uson, I., Pelikán, Sz., Tietze, L. F., Frank, É., Schneider, Gy., Acta Cryst. 1998, C54, 1341-1343. 88. Synthesis of Azasteroids and D-Homosteroids by Intramolecular Cyclization Reactions of Steroid Arylimines Wölfling, J., Frank, É., Schneider, Gy., Bes, M. T., Tietze, L. F. Synlett, 1998, 1205-1206. 89. Microwave-induced Selective Deacetylation and Stereospecific Acyl Migration of Steroid Acetates on Alumina Vass, A., Tapolcsányi, P., Wölfling, J., Schneider, Gy. J. Chem. Soc., Perkin Trans. 1 1998, 2873-2875. 90. Synthesis of Unusal Bridged Steroid Alkaloids by an Iminium Ion Induced 1,5-Shift of a Benzylic Hydride Wölfling, J., Frank, É., Schneider, Gy., Tietze, L. F. Angew. Chem. 1999.111, 151-152. Angew. Chem. Int. Ed. 1999, 38, 200-201. 91. High-performance Liquid Chromatographic Methods for Monitoring of Isomers of 17-Hydroxy-16-hydroxymethyl-3-methoxyestra-1,3,5(10)-triene Wölfling, J., Péter, A., Schneider, Gy. Journal of Chromatography A 1999, 852, 433-440.
92. Synthesis of Novel Steroid Alkaloids by Cyclization of Arylimines from Estrone Wölfling, J., Frank, É., Schneider, Gy., Tietze, L. F. Eur. J. Org. Chem. 1999, 3013-3020. 93. A Novel Approach in Drug Discovery: Synthesis of Estrone-Talaromycin Natural Product Hybrids Tietze, L. F., Schneider, Gy., Wölfling, J., Fecher, A., Nöbel, T., Petersen, S., Schuberth, I., Wulff, C. Chem. Eur. J. 2000, 6, 3755-3760. 94. A Steroidal Phenyldihydro-1,3-oxazine derivative Hewitt, M., Schneider, T.R., Szemerédi, Zs., Hajnal, A., Wölfling, J., Schneider, Gy. Acta Cryst. 2000, C56, e363-e364. 95. Configurational analysis and relative binding affinities of 16-methyl-5α-androstane derivatives Tapolcsányi, P., Wölfling, J., Tóth, I., Szécsi, M., Forgó, P., Schneider, Gy. Steroids 2001, 66, 833-843. 96. Neighboring Group Participation. Part 14. The preparation of the four stereoisomers of 16-hydroxymethyl-5α-androstane-3β,17-diol Tapolcsányi, P., Wölfling, J., Schneider, Gy. Steroids 2001, 66, 623-635. 97. Synthesis of Some Steroidal Oxazolines Wölfling, J., Mernyák, E., Sebõk, M., Schneider, Gy. Collect. Czech. Chem. Commun. 2001, 66, 1831-1840. 98. Halogéntartalmú és heterociklusos ösztronszármazékok szintézise Frank É., Wölfling, J., Schneider, Gy. Acta Pharm. Hung. 2001, 71, 441-447. 99. Synthesis and receptor binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers Tapolcsányi, P., Wölfling, J., Falkay, Gy., Márki, Á., Minorics, R., Schneider, Gy. Steroids, 2002, 67, 671-678. 100. Stereoselective Synthesis of New Halogen-containing D-Homoestrone Derivatives Frank, É., Mernyák, E., Wölfling, J., Schneider, Gy. Synlett, 2002, 419-422. 101. Novel Preparation of Dihydrooxazines Condensed to Ring D of the Estrane Skeleton Hajnal A., Wölfling, J., Schneider, Gy. Synlett, 2002, 1077-1080.
102. Stereoselective synthesis of some novel heterocyclic estrone derivatives by intramolecular 1,3-dipolar cycloaddition Frank, É., Wölfling, J., Aukszi, B., König, V., Schneider, T. R., Schneider, Gy. Tetrahedron 2002, 58, 6843-6849. 103. Synthesis of novel halogen-containing D-homoestrone and 13α-D-homoestrone derivatives by Lewis acid-induced intramolecular Prins reaction Wölfling, J., Frank, É., Mernyák, E., Bunkóczi, G., Cuesta Seijo, J. A., Schneider, Gy. Tetrahedron 2002, 58, 6851-6861. 104. Stereoselective Approach to some Novel 16-Methylated and 16-Halomethylated Tetrahydropyran and δ-Lactone Derivatives in both the Normal and the 13α-Estrone Series Frank, É., Mernyák, E., Wölfling, J., Schneider, Gy Synlett 2002, 1803-1806. 105. 3-Methoxy-1’-phenyl-4’β,5-dihydro-1H-pyrazolo[4’,3’:16,17]estra-1,3,5(10)-triene König, V., Schneider, T. R., Frank, É., Aukszi, B., Schneider, Gy., Wölfling, J. Acta Cryst. 2002, E58, 810-811. 105. Synthesis and receptor-binding examinations of the normal and 13-epi-Dhomoestrones and their 3-methyl ethers Wölfling, J., Mernyák, E., Frank, É., Falkay, Gy., Márki, Á., Minorics, R., Schneider, Gy. Steroids 2003, 68, 277-288. 106. Addition reactions at the 16(17) double bond of 3-methoxy-13α-estra-1,3,5(10),16tetraene Mernyák, E., Schönecker, B., Lange, C., Kötterizsch, M., Görls, H., Wölfling, J., Schneider, Gy. Steroids 2003, 68, 289-295. 107. Stereoselective halogenation of the 16-hydroxymethyl-3-methoxy-13α-estra-1,3,5(10)trien-17-ols and their solvolytic investigation Wölfling, J., Mernyák, E., Forgó, P., Schneider, Gy. Steroids 2003, 68, 451-458. 108. Stereoselective Synthesis of the Two trans-(16Hydroxymethyl)-3-methoxy-13α estra-1,3,5(10)-trien-17-ol Isomers Mernyák, E., Wölfling, J., Bunkóczi, G., Luo, L., Schneider, T. R., Schneider, Gy. Collect. Czech. Chem. Commun. 2003, 68, 1141-1148. 109. Synthesis of N-[2-(2-pyridyl)ethyl]-17a-aza-D-homosteroids and their biomimetic copper-mediated ligand hydroxylations with molecular oxygen Magyar, A., Schönecker, B., Wölfling, J., Schneider, Gy., Günther, W., Görls, H. Tetrahedron Asymmetry 2003, 14, 1925-1934.
110. Synthesis of 16,17-seco-steroids with iminomethyl-2-pyridine and aminomethylene-2Pyridine structures as chiral ligands for copper ions and molecular oxigen activation Magyar, A., Schönecker, B., Wölfling, J., Schneider, Gy., Günther, W., Görls, H. Tetrahedron Asymmetry 2003, 14, 2705-2715. 111. Synthesis of novel D-seco-pregnanes Wölfling, J., Magyar, A., Schneider, Gy. Monatshefte für Chemie 2003, 134, 1387-1393. 112. Novel medium ring sized estradiol derivatives by intramolecular Heck reactions Tietze, L., F., Sommer, K., M., Schneider, Gy., Tapolcsányi, P., Wölfling, J., Müller, P., Noltemeyer, M., Terlau, H. Synlett, 2003, 1494-1496. 113. Synthesis of Novel D-Secoestrone Isoquinuclidines by an Unpredicted Iminium IonInduced 1,5-Hydride Shift Wölfling, J., Frank, É., Schneider, Gy., Tietze, L., F. Eur. J. Org. Chem. 2004, 90-100. 114. Exo-heterociklusos szteroidok szintézise Schneider, Gy., Wölfling, J., Mernyák, E., Tóth, I. Magyar Kémiai Folyóirat 2004, 109-110, 40-42. 115. Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and D-homosteroids by inramolecular cyclization reactions Magyar, A., Wölfling, J., Kubas, M., Cuesta-Seijo, J., A., Sevvana, M., Herbst-Irmer, R., Forgó, P., Schneider, Gy. Steroids 2004, 69, 301-312. 116. Neighboring group participation Part 15. Stereoselective synthesis of some steroidal tetrahydrooxazin-2-ones, as novel presumed inhibitors of human 5α-reductase Wölfling, J., Hackler, L., Mernyák, E., Schneider, Gy., Tóth, I., Szécsi, M., Julesz, J., Sohár, P., Csámpai A. Steroids 2004, 69, 451-460. 117. Synthetic Cardenolides and Related Compounds Schneider, Gy., Wölfling, J. Current Organic Chemistry, 2004, 8, 1381-1403. 118. The Mitsunobu Inversion Reaction of Sterically Hindered 17-Hydroxy Steroids Tapolcsányi, P., Wölfling, J., Mernyák, E., Schneider, Gy. Monatshefte für Chemie 2004, 135, 1129-1136. 119. Stereoselective Synthesis of Condensed Aza-D-homo-estra Derivatives by 1,3-Dipolar Cycloaddition Mernyák, E., Benedek, G., Schneider, Gy., Wölfling, J. Synlett 2005, 637-639.
120.
Synthesis of Some Novel D-Dihomo-aza- and D-Dihomo-oxa-steroid Derivatives in the Estrone Series Frank, E., Schneider, Gy., Messinger, J., Thole, H., Wölfling, J. Synlett 2005, 2814-2816.
121.
Neighboring group participation Part 16. Stereoselective synthesis and receptorbinding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols Szájli, Á., Wölfling, J., Mernyák, E., Minorics, R., Márki, Á., Falkay, G., Schneider, Gy. Steroids 2006, 71, 141-153.
122.
Synthesis and stereochemical investigations of novel nitrogen-containing 13α-estrone derivatives Mernyák, E., Schneider, Gy., Herbst-Irmer, R., Kubas, M., Wölfling, J Steroids 2006, 71, 558-564.
123.
Stereoselective synthesis of some 17β-dihydrooxazinyl steroids, as novel presumed inhibitors of 17α-hydroxylase-C17,20-lyase Wölfling, J., Oravecz, É. A., Ondré, D., Mernyák, E., Schneider, Gy., Tóth, I., Szécsi, M., Julesz, J. Steroids 2006, 71, 809-816.
124.
Synthesis of D-seco-13α-Androst-5-ene Derivatives Wölfling, J. Szájli, Á., Vörös, L., Gáspár, M., Schneider, Gy. Monatshefte für Chemie 2006, 137, 1099-1107.
