Szerves Kémia és Technológia Tanszék
Vegyészmérnöki és Biomérnöki Kar

Könyv, könyvfejezet:

1.      Faigl, F., Kozma, D.: Optical Resolution via Complex Formation with O,O’-Dibenzoyltartaric Acid, in „Enantiomer Separation: Fundamentals and Practical Methods”, Chapter 3. (Edited by Toda, F.), Kluwer Academic Publishers, Dordrecht, Hollandia, 2004, pp 73-102.

2.      Marosi Gy., Keglevich Gy., Faigl F., Nelson G.: Development of the concepts of green chemistry in educational programs at Budapest University of Technology and Economics, in collaboration with Florida Institute of Technology. in “How science can support environmental protection? Florida Tech–BME Partnership Programme Yearbook” (Eds. Nelson G., Hronszky I.), Budapest, 2003, p. 175.

3.      F. Faigl, J. Schindler, E. Fogassy: Advantages of structural similarities of the reactants in  optical resolution processes, in Novel Optical Resolution Technologies, (editors: K. Sakai, N. Hirayama, R. Tamura) in the series of Topics in Current Chemistry, Vol. 269, Springer Berlin, Heidelberg, 2007, pp. 133-158. (SCI imp.f.: 4,163).

4.      Faigl, F., Mátravölgyi, B., Thurner, A.: Novel Methods for the Separation of Optical Isomers, in New Methodologies and Techniques for a Sustainable Organic Chemistry (Eds.: Mordini, A., Faigl, F.). NATO Science Series II: Mathematics, Physics and Chemistry, Vol. 246, Springer Berlin, Heidelberg, 2008, pp. 295-315, nyomdában. Paperback: 354 pages Publisher: Springer; 1 edition (March 2008) Language: English ISBN-10: 1402067925 ISBN-13: 978-1402067921 A teljes könyv társszerkesztője is.

5.      E. Pálovics, F. Faigl, E. Fogassy: Separation of the Mixtures of Chiral Compounds by Crystallization, Chapter 1 in Advances in Crystallization Processes (edited by Yitzhak Mastai), ISBN 978-953-51-0581-7, InTech.  Available from: http://www.intechopen.com/books/advances-in-crystallization-processes/th.... (2012) pp 1-36. DOI: 10.5772/33592

6.      E. Pálovics, J. Schindler, F. Faigl, E. Fogassy: Behavior of Structurally Similar Molecules in the Resolution Processes. In Comprehensive Chirality (E.M. Carreira, H. Yamamoto eds), Vol. 8: Separations and Analysis (G.E. Traner vol. ed.), Elsevier, Amsterdam, 2012, pp 91-96.

Jelentősebb közlemények (2000-2015):

1.         Faigl, F., E. Marzi, Schlosser, M.: Chemistry, A European Journal 6(5), 771 (2000). (Enhancement of Benzylic Basicity by a Fluorine Substituent at the para Position)

2.         Fogassy, K., Harmat, V., Böcskei, Zs., Tárkányi, G., Tőke, L., Faigl, F.: Tetrahedron: Asymmetry 11(23), 4771-4780 (2000). (Efficient Synthesis and Optical Resolution of (±)-1-[2-Carboxy-6-(trifluoromethyl)-phenyl]pyrrole-2-carboxylic Acid.)

3.         Faigl, F., Thurner, A., Kovári, J., Tárkányi, G., Tőke, L., Mordini, A.: Tetrahedron: Asymmetry, 13, 59-68 (2002). (Resolution and Enantioselective Rearrangements of Amino Group Containing Oxiranyl Ethers.)

4.         Tilly, D., Samanta, S.S., Faigl, F., Mortier, J.: Tetrahedron Letters, 43 (46), 8347-8350, (2002). (Combined directed ortho metalation-intramolecular Friedel–Crafts connections. Regiospecific route to 1-substituted fluoren-9-ones.)

5.         Ágai, B., Proszenyák, Á., Tárkányi, G., Vida, L., Faigl, F. Eur. J. Org. Chem. 2004, 3623-3632. (Convenient, bening and scalable synthesis of 2- and 4-(substituted-benzyl)piperidines.)

6.         F. Faigl, A. Thurner, M. Battancs, F. Farkas, L. Poppe, V. Bódai, I. Kmecz, B. Simándi: Tetrahedron: Asymmetry, 16, 3841-3847 (2005). (Efficient, scalable kineticresolution of cis-4-benzyloxymethyl-2,3-epoxybutanol.)

7.         F. Faigl,B.Vas Feldhoffer, A. Thurner: Synth. Commun. 36, 2841-2849 (2006). (Organometallic Approach to the Functionalization of Alkyl Groups Containing 1-Phenylpyrroles).

8.         F. Faigl, A. Thurner, F. Farkas, M. Battancs, L. Poppe: Chirality 19, 197-202 (2007) (Synthesis and enantioselective rearrangement of (Z)-4-triphenylmethoxy-2,3-epoxybutan-1-ol enantiomers.)

9.         Faigl, F., Fogassy, E., Nógrádi, M., Pálovics, E., Schindler, J.: Tetrahedron: Asymmetry 19, 519-536 (2008). (review, Strategies in optical resolution: a practical guide).

10.       F. Faigl, E. Kovács, G. Turczel, Á. Szöllősy, L. Balázs, T. Holczbauer, M. Czugler, A. Mordini: Tetrahedron: Asymmetry 23, 1607-1614 (2012). (Novel stereoselective synthesis of 1,2,3-trisubstituted azetidines.)

11.       Besenyei G., Bitter I., Párkányi L., Szalontai G., Baranyai P., Kunsági-Máté É., Faigl F., Grün A., Kubinyi M.: Polyhedron 55, 57–66 (2013) (A new xantphos-type ligand and its gold(I)complexes: Synthesis, structure, luminescence).

12.       133. E. Pálovics, Zs. Szeleczky, B. Fődi, F. Faigl, E. Fogassy: RSC Advances, 2014, 4, 21254-21261. (Prediction of the efficiency of diastereoisomer separation on the basis of the behaviour of enantiomeric mixtures.)

13.       E. Kovács, F. Faigl, Z. Mucsi, M. Nyerges, L. Hegedűs: J. Mol. Catal. A Chemical 395, 217-224 (2014). (Hydrogenolysis of N- and O-protected hydroxyazetidines over palladium: Efficient and selective methods for ring opening and deprotecting reactions).

14.       F. Faigl, Zs. Erdélyi, Sz. Deák, M. Nyerges, B. Mátravölgyi: Tetrahedron Letters 55(50), 6891-6894 (2014). DOI: http://dx.doi.org/10.1016/j.tetlet.2014.10.101 (A new pyrrolidine-derived atropisomeric amino alcohol as a highly efficient chiral ligand for the asymmetric addition of diethylzinc to aldehydes.)

15.       F. Faigl, Sz. Deák, Zs. Erdélyi, T. Holzbauer, M. Czugler, M. Nyerges, B. Mátravölgyi Chirality 27(3), 216-222 (2015). (New Atropisomeric Amino Alcohol Ligands for Enantioselective Addition of Diethylzinc to Aldehydes.).