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Dr. Ferenc Faigl; PhD, DSc
full professor
Contact info
Office: 
F. II. ground floor 5.
Laboratory: 
F. II. ground floor 6.
Telephone: 
+36 1 463 3652
+36 1 463 1111/5889
Fax: 
+36 1 463 3648
Postal address: 
1521 Budapest, Pf. 91.
E-mail: 
Contact person by email
Research group
Innovative Pharmaceutical and Chirotechnological Research Group
Professional data
Research interests: 
  • Preparation of optically active compounds. Investigation of the behaviours of enantiomeric mixtures, development of resolution methods
  • Investigation of stereoselective reactions
  • Investigation of the reactions of polar organometallics
  • Application of the research findings in development of environmentally benign processes for pharmaceutical and fine chemical industries
Scientific degrees: 

1996: Doctor of Chemical Sciences (D. Sc.), (Separation of optical isomers via diastereoisomeric salt formation)
1996: Habilitation (BME Faculty of Chemical Engineering, Chemistry of polar organometallics)
1981: University doctor (dr. techn.), (Synthesis of optically active phenylglycine derivatives)

Studies, degrees: 

1977: Dipl. Chemical engineer (M. Sc.), BME Faculty of Chemical Engineering, Department of Organic Chemical Technology

Workplaces, positions: 

From 1997: full professor (BME Department of Organic Chemistry and Technology): Separation of racemic and non racemic enantiomeric mixtures, investigation of chiral supramolecular structures; regio and stereoselective reactions of polar organometallics, synthesis and application of chiral ligands; development of novel organic technologies for pharmaceutical industries.

1996-1997: associate professor (BME Department of Organic Chemistry and Technology): Separation of optical isomers, preparation and synthetic application of organolithium compounds.

1984-1996: research fellow (MTA-BME Organic Chemical Technology Research Group): development of pH-controlled resolutions via diastereoisomeric salt formation, resolution of racemates with structurally similar resolving agents, development of new methods for enantiomer separation of chiral amines, carboxylic acids and amino acid derivatives; development of regioselective metalation methods.

1977-1984: assistant research fellow (MTA-BME Organic Chemical Technology Research Group): Investigation of the separation efficiency-chemical structure realtionships during resolution and second order asymmetric transformations via distereoisomeric salt formation, development of the thermodinamic equilibrium model of resolution via diastereoisomeric salt formation.

Visits: 

1 month or longer professional stay abroad:
1990-1992: Postdoctoral fellowship, Institute of Organic Chemistry, Lausanne University, Switzerland (26 months, Group of Professor Manfred Schlosser)
1994: Visiting researcher, Institute of Organic Chemistry, Lausanne University, Switzerland (3 months, Group of Professor Manfred Schlosser)
1996: Visiting professor, Institute of Organic Chemistry, Lausanne University, Switzerland (2 months, Group of Professor Manfred Schlosser)

Short professional stays abroad:
Referee of PhD Theses (Lausanne University, 1998, 2003) invited lecturer, expert (Firmenich Ltd, Genf, Switzerland 1999; Lausanne University 2001; Lonza Group Ltd., Brig, Switzerland 2001; Dijon University, France 2001; Zentiva Ltd, Prague, Czech 2013).

 

Education
Teaching types: 

Development and direction of laboratory courses, lecturer of different subjects for BSc and MsC students as well as teaching of postgraduate and PhD students.
Member of the Board of Final Examinations at BSc and MSc levels, pharmaceutical industry branch.
President of the Board of Final Examinations at BSc and MSc level, pharmaceutical industry branch.

Regular teaching: 

BSc level:
„Industrial Organic Chemistry”, 1984-1987
„Basic Processes in Pharmaceutical Chemistry” from 1995
„Medicines” from 1998

MSc level:
„Chemistry and Technology of Polar Organometallics” from 1995
„Projects in Organic Chemistry”, superviser since 2000;
„Medicinal Chemistry” from 2003

PhD courses:
„Chirotechnology”, 2002-2010
„Unit Processes and Tehcnologies in Pharmaceutical Industryy” from 2002.

Teaching method/topic development: 
  • Leader of the reorganization and development of the environmental engineering education (BSc and MSc levels, 2014.2015)
  • Participation in the development of multigrade education system (BSc-MSc-PhD) at the Faculty of Chemical Technology and Biotechnology, 2000-2001; participation in foundation of „Engineer in Pharmaceutical Industry” MSc branch.
  • Development of subjects: „Medicines” for BSc students, „Chemistry and Technology of Polar Organometallics” for MSc students.
  • Students’ books (in Hungarian): ­
    • Faigl, F.: co-author, "Szerves vegyipari alapfolyamatok gyakorlat" (szerk.: Fenichel, L.) egyetemi jegyzet, J6-945, Tankönyvkiadó, Budapest 1990. ­
    • Faigl, F.:A főcsoportbeli fémek szerves származéka i“Szerves fémvegyületek kémiája” II. fejezet, (szerk.: Kollár, L.), Nemzeti Tankönyvkiadó, Budapest, 2001, 111-206. old. ­
    • Faigl, F., Kovács, E., Mátravölgyi, B., Thurner, A.: Gyógyszerkémiai alapfolyamatok, egyetemi e-tankönyv (szerk.: Faigl F.), Typotex, Budapest, 2011, ISBN 978-963-279-477-8. http://www.interkonyv.hu/konyvek/ ­
    • Faigl, F., Szeghy, L., Kovács, E., Mátravölgyi, B.: Gyógyszerek, egyetemi e-tankönyv (szerk.: Faigl F.), Typotex, Budapest, 2011, ISBN 978-963-279-476-1. http://www.interkonyv.hu/konyvek/
Academic administration
Scientific organisation memberships: 
  • Member of the Society of Hungarian Scientists and Scholars, Hungarian Academy of Sciences (from 1997)
  • Member of the Hungarian academy of Engineers (from 2004)
International scientific organisation: 

COST D40 member of the Management Committee 2006-2010
Vice director of summer university organized with the aid of NATO ASI: NeMeTOC, Siena, Italy 2005

Committee membership, Academy of Sciences: 
  • MTA Working Committee for Heterocyclic and Elemental Organic Chemistry (2006-2010)
  • MTA Committee of Organic and Biomolecular Chemistry (from 2014)
  • Council of the Leaders of the MTA Research Institutions (elected member from 2012).
Editorial board member: 

The Open Organic Chemistry Journal (since 2011)

Guest editor: 

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.

Referee activity: 

Tetrahedron, Tetrahedron Letters, Tetrahedron: Asymmetry,l Chirality, Journal of Organic Chemistry, Monatschefte für Chemie, Open organic Chemistry Journal, etc.

Conference organisation: 

  • "3rd COST D2 Working Group Meeting on CF3 Chemistry" international symposium with the participation of researchers of six countries, 1995, Budapest
  • "Synthetic Applications of Polar Organometallics" mini-symposium and COST cooperation preparatory meeting, 2000, Budapest
  • NATO ASI New Methodologies and Technics in Organic Chemistry: Sustaniable Development in a Secure Environment (NeMeTOC), Sienna, Certosa di Pontignano, 2005 október 14-23.
Activity in scientific evaluations: 

Referee and member of evaulating committees for PhD Theses, Habilitation Theses, D.Sc. Theses
European and national competitions since 1998 (BME, ELTE, SzIE ÁOTK, MTA, UNIL, EPFL, etc.)
Juryman at Hungarian Scientific research Fund (OTKA, 2012-2015)

Leadership
University, Faculty, Department mandates: 

From 2013 Dean, BME faculty of Chemical technology and Biotechnology, member of the BME University Senate
2004-2006 member of the BME University Senate
1999-2011 Deputy dean, BME faculty of Chemical technology and Biotechnology
From 2002 Head of the MTA-BME Organic Chemical Technology Research Group
1997-2013 Deputy head of the BME Department of Organic Chemistry and technology
From 2003 member of the Habilitation Committee and Doctoral Council of Faculty of Chemical Technology and Biotechnology

Scientific project co-ordination: 

Hungarian projects:

OTKA T 104528 (2012-2016) leader, BME Kutatóegyetemi pályázat: Új Széchenyi terv (TÁMOP-4.2.1/B-09/1/KMR-2010-0002) participant,OTKA T048362 (2005-2008) leader, OTKA T030803 (1999-2002) leader, OTKA T014932 (1995-1998) leader, OTKA M 36458 (2001) leader; GVOP-3.3.2.-2004-07-006/3.0 pályázat 2.6. projekt (2005-2007) participant, NKFP, 3A/35/2003 konzorciumi pályázat 5/3, 9, 15 projekt (2002-2005) participant.

International projects:

COST D40 (2007-2011) Management Committee member; COST D24/0006/02 (2003-2006) Hungarian project leader; NATO ASI, PST.MEM.ASI.980850 (2005-2007) summer university vice president; CNR (Firenze)/MTA bilateral research cooperation (1996-2015) Hungarian prject leader, Lengyel tud. Akadémia (Varsó)/MTA bilateral research cooperation (1995-1998) Hungarian project leader, COST D2 (1994-1997) Hungarian project leader.
Contract projects : 

Since 1997 participant and project leader of numerous research and development projects with industrial partners (Alkaloida, Chinoin, EGIS, Richter, TEVA, Sanofi-Zentiva)

Scientific and teaching awards
  • Awards of Hungarian Academy of Sciences for young researchers (1986, 1990)
  • Gold degree of outstanding inventors two times: 1987 and 1989 (from the Hungarian Patent Office)
  • “Jedlik Ányos” award (from the Hungarian Patent Office, 2007)
  • “Zemplén Géza” (from the Hungarian Academy of Sciences, 2007)
  • Knight of Cross from the Order of Merit of the Hungarian Republic (President of Hungary, 2010)
Publications
Summary of scientific achievements: 

Co-author of 3 book chaptersand 2 books in Hungarian, 5 book chapters in English, editor of 2 books in hungarian and 1 in English; - 140 Articles (IF ~157, H-index: 19, citations 1060, indep. citations ~ 680) - 51 Patents and patent applications (National and international) -~ 170 Conference lectures / posters

Selected publications: 

Book, chapters:

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.

 

Selected publications (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.).

Detailed list of publications in databases
Hungarian Scientific Bibliography database (MTMT): 
https://vm.mtmt.hu//search/slist.php?lang=0&AuthorID=10008354
BUTE Publication database (BME PA): 
http://mycite.omikk.bme.hu/search/slist.php?lang=0&AuthorID=10004096
Last modified: 
2024 May 23 - 14:11