Lázár László tudományos közleményeinek idézettsége

Átírás

1 Lázár László tudományos közleményeinek idézettsége (2011. szeptember 23-i állapot; idézések száma: 477) Ferenc Fülöp, László Lázár, István Pelczer, Gábor Bernáth: One-pot synthesis of partially saturated tetracyclic benzoxazines; scope and limitations Tetrahedron 44, (1988) 1. J. L. Gras et al.: Bull. Soc. Chim. Fr. 131, 418 (1994) 2. A. Star et al.: Angew. Chem. Int. Ed. Eng. 39, 2685 (2000) 3. A. Star et al.: J. Organomet. Chem. 630, 67 (2001) 4. F. Laduron et al.: Org. Proc. Res. Dev. 9, 102 (2005) Fülöp Ferenc, Lázár László, Bernáth Gábor, Pelczer István: Részlegesen telített tetraciklusos benzoxazinok egylombikos szintézise Magy. Kém. Foly. 95, (1989) 1. Houben-Weyl: Methoden der organishen Chemie, Band E 14a/Teil 2, O/N-Acetale, Herausgegeben von H. Hagemann, D. Klamann Georg Thieme Verlag, Stuttgart, New York, 1991, p R. P. Subrayan, F. N. Jones: Chemistry of Materials 10, 3506 (1998) 3. C. Schaller, P. Vogel: Synlett 1219 (1999) 4. C. Schaller, P. Vogel: Helv. Chim. Acta 83, 193 (2000) 5. E. V. Gromachevskaya et al.: Khim. Geterosikl. Soedin. 163 (2003) Ferenc Fülöp, László Lázár, Mohamed S. A. El-Gharib, Gábor Bernáth: Synthesis of 1,5,6,10b-tetrahydro-1,2,4-triazolo[3,4-a]isoquinolines Pharmazie 45, (1990) 1. A. S. Shawali: Chem. Rev. 93, 2731 (1993) 2. H. A. Abelhadi et al.: J. Chem. Res. (S) 292 (1996) 3. A. Linden et al.: Acta Cryst., Sect. C 58, o122 (2002) 4. E. M. Awad et al.: Helv. Chim. Acta 85, 320 (2002) 5. A. S. Shawali, M. A. N. Mosselhi: J. Heterocyclic Chem. 40, 725 (2003) 6. H. M. Hassaneen et al.: Z. Naturforsch. B 66, 299 (2011) László Lázár, Ferenc Fülöp, György Dombi, Gábor Bernáth, Gyula Argay, Alajos Kálmán: Preparation and conformational analysis of stereoisomeric 1,6,7,11b-tetrahydro-2H- 1,3-oxazino[4,3-a]isoquinolines Tetrahedron 46, (1990)

2 I. Hermecz, L. Vasvári-Debreczy: Bicyclic 6-6 Systems with One Ring Junction Nitrogen Atom: One Extra Heteroatom 1:0, in Comprehensive Heterocyclic Chemistry II, Review of the Literature (Eds.: A. R. Katritzky, C. W. Rees, E. F. Scriven), Pergamon Press, Glasgow, 1996, Vol. 8, p I. Hermecz: Adv. Heterocyclic Chem. 70, 1 (1998) 3. Z. Kaluza et al.: Tetrahedron 56, 5553 (2000) 4. C. Fuchs et al.: J. Heterocyclic Chem. 45, 1651 (2008) Lázár László, Fülöp Ferenc, Dombi György, Bernáth Gábor, Argay Gyula, Kálmán Alajos: Sztereoizomer 1,6,7,11b-tetrahidro-2H-1,3-oxazino[4,3-a]izokinolin-4-on származékok szintézise és konformációanalízise Magy. Kém. Foly. 96, (1990) 1. M. F. Brana et al.: J. Org. Chem. 61, 1369 (1996) László Lázár, Ferenc Fülöp, Gábor Bernáth, Alajos Kálmán, Gyula Argay: Synthesis and stereochemistry of steroisomeric 1,3-benzoxazino-1,3- and -3,1- benzoxazines J. Heterocyclic Chem. 28, (1991) 1. E. V. Gromachevskaya et al.: Khim. Geterosikl. Soedin. 163 (2003) 2. E. V. Gromachevskaya et al.: Khim. Geterosikl. Soedin (2006) 3. M. Ghandi et al.: J. Heterocyclic Chem. 46, 914 (2009) Bernáth Gábor, Fülöp Ferenc, Kiss Béla, Kárpáti Egon, Pálosi Éva, Lapis Erzsébet, Gere Anikó, Szabó Sándor, Huber Imre, Kóbor Jenı, Lázár László, Sarkadi Ádám, Szombathelyi Zsolt, Szporny László, Csomor Katalin, Árva Judit, Bodó Mihály, Laszy Judit, Szentirmai Zsolt: Eljárás szubsztituált oxazino-izokinolin-származékok és az ezeket tartalmazó gyógyászati készítmények elıállítására Hung. Pat , 12 December 1991; Chem Abstr. 119, p (1993) 1. I. Hermecz: Adv. Heterocyclic Chem. 70, 1 (1998) Pál Sohár, László Lázár, Ferenc Fülöp, Gábor Bernáth, Jenı Kóbor: Synthesis and conformational analysis of stereoisomeric 1- and 2-methyl-2H,4H- 1,6,7,11b-tetrahydro-1,3-oxazino[4,3-a]isoquinolines Tetrahedron 48, (1992) 1. I. Hermecz, L. Vasvári-Debreczy: Bicyclic 6-6 Systems with One Ring Junction Nitrogen Atom: One Extra Heteroatom 1:0, in Comprehensive Heterocyclic Chemistry II, Review of the Literature (Eds.: A. R. Katritzky, C. W. Rees, E. F. Scriven), Pergamon Press, Glasgow, 1996, Vol. 8, p S.-D. Cho et al.: Tetrahedron 60, 3763 (2004)

3 C. Fuchs et al.: J. Heterocyclic Chem. 45, 1651 (2008) László Lázár, Ferenc Fülöp, Gábor Bernáth, Jorma Mattinen: A simple synthesis of 1-hydroxyalkyl-1,2,3,4-tetrahydroisoquinolines Org. Prep. Proc. Int. 25, (1993) 1. M. Balasubramanian, E. F. V. Scriven: Isoquinoline and its derivatives, In: Rodd s Chemistry of Carbon Compounds, Second Supplements to the 2 nd Edition, Vol. IV, Part F/G, Elsevier, Amsterdam, 1998, p.163 Ferenc Fülöp, László Lázár, Gábor Bernáth, Reijo Sillanpää, Kalevi Pihlaja: Substituent effects on the ring-chain tautomerism of 1,3-oxazines Tetrahedron 49, (1993) 1. J. M. McGill, R. Johnson: Tetrahedron 50, 3857 (1994) 2. D. Miguel et al.: Tetrahedron 51, 7527 (1995) 3. S. D. Derrick et al.: Tetrahedron 52, 7679 (1996) 4. M. Sainsbury: 1,3-Oxazines and their Benzo Derivatives, in Comprehensive Heterocyclic Chemistry II, Review of the Literature (Eds.: A. R. Katritzky, C. W. Rees, E. F. Scriven), Pergamon Press, Glasgow, 1996, Vol. 6, p T. Sakai et al.: Tetrahedron Letters 38, 1987 (1997) 6. M. Sainsbury: 1,3-Oxazines and benzoxazines, In: Rodd s Chemistry of Carbon Compounds, Second Supplements to the 2 nd Edition, Vol. IV, Part G/H, Elsevier, Amsterdam, 1998, p K. Singh et al.: Tetrahedron 54, 3567 (1998) 8. L. Joubran et al.: Austr. J. Chem. 56, 597 (2003) 9. E. Kleinpeter: Adv. Heterocyclic Chem. 86, 41 (2004) 10. R. Pedrosa et al.: Chiral perhydro-1,3-benzoxazines: Powerful auxiliaries in asymmetric synthesis of nitrogen heterocycles, in New Methods for the Asymmetric Synthesis of Nitrogen Heterocycles (Eds.: J. L. Vicario, D. Badia, L. Carrillo), Research Signpost, Trivandrum, 2005, p M. Panunzio et al.: Tetrahedron 62, (2006) N. De Kimpe, M. Boeykens, L. Lázár, Z. Szakonyi, A. Kemme, G. Duburs: Rearrangement and cyclization of β-mesyloxy ketones. Synthesis of δ-sultones Bull. Soc. Chim. Belg. 103, (1994) 1. P. Metz: J. Prak. Chem. - Chem. Ztg. 340, 1 (1998) Norbert De Kimpe, Angelina Georgieva, Marc Boeykens, László Lázár: Synthesis of laurencione, a labile dihydro-3(2h)-furanone derivative from the red alga Laurencia spectabilis J. Org. Chem. 60, (1995) 1. D. J. Faulkner: Nat. Prod. Reports 14, 259 (1997)

4 E. Wolf et al.: Can. J. Chem. 75, 942 (1997) 3. S. R. Putra et al.: Tetrahedron Letters 39, 6185 (1998) 4. D. G. McCarthy et al.: J. Chem. Soc., Perkin Trans (1999) 5. C. Cerny, T. Davidek: J. Agr. Food Chem. 51, 2714 (2003) 6. D. Alvarez-Dorta et al.: Angew. Chem. Int. Ed. 47, 8917 (2008) 7. M. Terada, K. Ando: Org. Letters 13, 2026 (2011) László Lázár, Attila G. Lakatos, Ferenc Fülöp, Gábor Bernáth, Frank G. Riddell: Five-component equilibria of ring-chain tautomeric mixtures derived from 3-amino- 1,2-propanediol and aromatic aldehyde Tetrahedron 53, (1997) 1. L. Carrillo et al.: J. Org. Chem. 62, 6716 (1997) 2. L. Carrillo et al.: Tetrahedron: Asymmetry 9, 151 (1998) 3. A. Star, B. Fuchs: J. Org. Chem. 64, 1166 (1999) 4. K. Singh, P. K. Deb: Heterocycles 51, 1509 (1999) 5. K. Singh, P. K. Deb: Tetrahedron Letters 41, 4977 (2000) 6. C. Hajji et al.: Tetrahedron 56, 8173 (2000) 7. K. Singh et al.: Tetrahedron 57, 7939 (2001) 8. C. Distaso et al.: WO (2001) 9. C. Hajji et al.: Tetrahedron 58, 3281 (2002) 10. E. Anakabe et al.: Chiral β-amino alcohols and derivatives in the asymmetric synthesis of tetrahydroisoquinolines, in: Targets in Heterocyclic Systems, Vol. 6, Societa Chimica Italiana, 2002, p C. Hajji et al.: Synth. Commun. 33, 4347 (2003) 12. S. Perez et al.: J. Org. Chem. 70, 4857 (2005) 13. V. Capriati et al.: Tetrahedron Letters 48, 8655 (2007) 14. D. Talancon et al.: J. Org. Chem. 75, 3294 (2010) László Lázár, Tamás Martinek, Gábor Bernáth, Ferenc Fülöp: A simple synthesis of β-alkyl-substituted β-amino acids Synth. Commun. 28, (1998) 1. A. S. Franklin: J. Chem. Soc., Perkin Trans (1999) 2. C. Tomasini, A. Vecchione: Org. Lett. 1, 2153 (1999) 3. G. C. Barrett: Amino Acids, Peptides and Proteins 31, 1 (2000) 4. D. J. Bayston et al.: US (2001) 5. A. Péter: J. Chromatography A 955, 141 (2002) 6. C. Y. K. Tan, D. F. Weaver: Tetrahedron 58, 7449 (2002) 7. E. Zarbl et al.: J. Separation Sci. 25, 1269 (2002) 8. G. R. Srinivasa et al.: Synth. Commun. 33, 4221 (2003) 9. G. R. Srinivasa et al.: Ind. J. Chem. B43, 192 (2004) 10. H. S. Prasad et al.: Synt. Commun. 35, 1189 (2005)

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6 V. Kysil et al.: Eur. J. Org. Chem (2010) Lázár László, Fülöp Ferenc: Győrő-lánc tautoméria alkalmazása prodrug szerek fejlesztésére Acta Pharm. Hung., 69, (1999) 1. J. Selambarom et al.: Tetrahedron 58, 9559 (2002) 2. C. Saiz et al.: J. Org. Chem. 76, 5738 (2011) Anikó Göblyös, László Lázár, Ferenc Evanics, Ferenc Fülöp: Substituent effects in the ring-chain tautomerism of 1,2-diarylimidazolidines Heterocycles 51, (1999) 1. A. Salerno et al.: Synth. Commun. 33, 3193 (2003) 2. J. A. Bisceglia et al.: J. Heterocyclic Chem. 41, 85 (2004) 3. I. Perillo et al.: Synthesis 851 (2004) 4. O. Maloshitskaya et al.: Tetrahedron 60, 6913 (2004) 5. A. W. Murray: Molecular rearrangements, in Organic Reactions Mechanisms 1999 (Eds.: A. C. Knipe and W. E. Watts), Wiley, Chichester, 2004, p I. Perillo et al.: Eur. J. Med. Chem. 40, 811 (2005) 7. N. Xi ez al: Imidazoles, in Comprehensive Heterocyclic Chemistry III (Eds.: A. R. Katritzky, C. A. Ramsden, E. F. V Scriven, R. J. K. Taylor), Elsevier, Amsterdam, 2008, Vol. 4, p. 143 Ferenc Fülöp, Márta Palkó, Judit Kámán, László Lázár, Reijo Sillanpää: Synthesis of all four enantiomers of 1-aminoindane-2-carboxylic acid, a new cispentacin benzologue Tetrahedron: Asymmetry 11, (2000) 1. D. J. Aitken et al.: Tetrahedron Letters 43, 6177 (2002) 2. L. K. Mehta; J. Parrick: Progress in Heterocyclic Chemistry 14, 75 (2002) 3. M. C. Whisler, P. Beak: J. Org. Chem. 68, 1207 (2003) 4. Z. C. Gyarmati et al.: Tetrahedron: Asymmetry 14, 3805 (2003) 5. Z. C. Gyarmati et al.: Adv. Synth. Catal. 346, 566 (2004) 6. A. A. Fuller et al.: J. Am. Chem. Soc. 127, 5376 (2005) 7. A. Liljeblad; L. T. Kanerva: Tetrahedron 62, 5831 (2006) 8. A. Mondière et al.: Tetrahedron 64, 1088 (2008) 9. E. Busto et al.: Chem. Rev. 111, 3998 (2011) Pál Sohár, Enikő Forró, Ferenc Fülöp, László Lázár, Gábor Bernáth, Reijo Sillanpää: Synthesis and stereochemistry of stereoisomeric 1,2,3-oxathiazino[4,3-a]- isoquinolines J. Chem. Soc. Perkin Trans (2000) 1. S.-D. Cho et al.: Tetrahedron 60, 3763 (2004)

7 E. Juaristi et al.: Dioxazines, oxathiazines, and dithiazines, in Comprehensive Heterocyclic Chemistry III (Eds.: A. R. Katritzky, C. A. Ramsden, E. F. V Scriven, R. J. K. Taylor), Elsevier, Amsterdam, 2008, Vol. 9, p P. Mátyus, P. Tapolcsányi: Bicyclic 6-6 systems with one bidgehead (ring junction) nitrogen atom: two extra heteroatoms 2:0, in Comprehensive Heterocyclic Chemistry III (Eds.: A. R. Katritzky, C. A. Ramsden, E. F. V Scriven, R. J. K. Taylor), Elsevier, Amsterdam, 2008, Vol. 12, p. 219 Szilvia Gedey, Arto Liljebad, László Lázár, Ferenc Fülöp, Liisa T. Kanerva: Preparation of highly enantiopure β-amino esters by Candida antarctica lipase A Tetrahedron: Asymmetry 12, (2001) 1. A. Péter: J. Chromatography A 955, 141 (2002) 2. O. Kirk, M. W. Christensen: Org. Process Res. Dev. 6, 446 (2002) 3. M. Liu, M. P. Sibi: Tetrahedron 58, 7991 (2002) 4. Z. H. Ma et al.: Chinese J. Org. Chem. 22, 807 (2002) 5. U. Hanefeld: Org. Biomol. Chem. 1, 2405 (2003) 6. T. Jerphagnon et al.: Tetrahedron: Asymmetry 14, 1973 (2003) 7. F. van Rantwijk, R. A. Sheldon: Tetrahedron 60, 501 (2004) 8. H. Groger et al.: Org. Biomol. Chem. 2, 1977 (2004) 9. C. Pousset et al.: Tetrahedron: Asymmetry 15, 3407 (2004) 10. M. Nejman et al.: Tetrahedron 61, 8536 (2005) 11. P. D. de Maria et al.: J. Mol. Catal. B-Enzym. 37, 36 (2005) 12. D. O. Berbasov et al.: Biocatalytic entry to enantiomerically pure β-amino acids, in Enantioselective Synthesis of β-amino Acids (Eds.: E. Juaristi; V. A. Soloshonok), 2 nd ed., Wiley, Hoboken, 2005, p M. G. Perrone et al.: Bioorg. Med. Chem. 14, 1207 (2006) 14. V. Gotor-Fernandez; V. Gotor: Curr. Org. Chem. 10, 1125 (2006) 15. A. Trusek-Holownia; A. Noworyta: J. Biotechnol. 130, 47 (2007) 16. V. Gotor-Fernández et al.: Preparation of chiral pharmaceuticals through enzymatic acylation of alcohols and amines, in Biocatalysis in the Pharmaceutical and Biotechnology Industries (Ed.: R. N. Patel), CRC Press, Boca Raton, 2007, p D. J. Ericsson et al.: J. Mol. Biol. 376, 109 (2008) 18. H.-E. Högberg: Exploiting enantioselectivity of hydrolases in organic solvents, in Organic Synthesis with Enzymes in Non-Aqueous Media (Eds.: G. Carrea; S. Riva), Wiley-VCH, Weinheim, 2008, p C. Bruneau et al.: Coord. Chem. Rev. 252, 532 (2008) 20. C. Wolf: Dynamic Stereochemistry of Chiral Compounds, The Royal Society of Chemistry, Cambridge, 2008, p M. K. J. ter Wiel et al.: Tetrahedron Asymmetry 20, 478 (2009) 22. A. G. Sandstrom et al.: Protein Engineering Design & Selection 22, 413 (2009)

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