1. Born:

October 6th, 1950, Pabianice, Poland

2. Education:

1964-1969 - Chemical High School in Pabianice
1969-1974 - Chemistry study at the Faculty of Mathematics, Physics and Chemistry (University of úˇd╝, Poland)
1982 - PhD thesis entitled: 'Reactions of Phenylmethylene with Imines' (supervisor: Prof. Romuald Bartnik) (University of úˇd╝).
1991 - Habilitation 'Thioketones and their S-Methylides' (University of úˇd╝).

3. Current positions

Since 1998 - Full professor at the University of úˇd╝
Since 1999 - Head of the Section of Heteroorganic Compounds
Since 2003 - Head of the Department of Organic and Applied Chemistry at the Faculty of Chemistry, University of úˇd╝

4. Scientific interest:

Organic synthesis, reaction mechanisms, heterocyclic and heteroatom chemistry, the organic chemistry of sulfur, 1,3-dipolar cycloadditions, hetero-Diels-Alder chemistry, heterocyclic N-oxides, the organic chemistry of fluorine, congested systems, heterocumulenes, flash vacuum pyrolysis, carbenes (including nucleophilic carbenes NHC) and nitrenes .

5. Activities abroad:

1983-1985; 1987-1988 - University of Munich (Germany); Alexander von Humboldt Fellow in the research group of Prof. Rolf Huisgen.
1995 - University of Zurich (Switzerland); Swiss Government Fellow in the research group of Prof. Heinz Heimgartner (3 monthes).
1996-1997 - University of Southern California (USA); Distinguished Scholar at Loker Hydrocarbon Institute; research group of Nobel Prize Laureate 1994, Prof. George A. Olah.
2004 - Free University Berlin (Germany) -Visiting Professor, Humboldt Fellow in the research group of Prof. H. U. Reissig.
1987-2008 - Justus Liebig University (Giessen, Germany) - Visiting professor in the research groups of Prof. Prof. G. Maier and subsequently prof. P. R. Schreiner.

6. Other activities

Dean of the Faculty of Chemistry, University of úˇd╝ (2012-2016).
Vice Dean of the Faculty of Mathematic, Physics & Chemistry (University of úˇd╝) - (1993-1996).
Member of 'Senat' of the University of úˇd╝ (2012-2016).
Member of the Executive Committee of the Polish Chemical Society (2001-2009)
Member of the Editorial Boards of Sulfur Letters and Sulfur Reports(until 2004; at currently under new tile: Journal of Sulfur Chemistry) and Phosphorus, Sulfur, and Phosphorus Sulfur Silicon Rel. Element.

7. Current collaborations with foreign groups:

Prof. H. Heimgartner, University of Zurich (Switzerland), Prof. W. Weigand, University of Jena (Germany), Prof. P. R. Schreiner (University of Giessen (Germany), Prof. M. Gulea University of Caen (France).

8. Scientific achievements:

Over 300 original papers, 36 review articles, 6 patents, > 400 symposia presentations, > 50 invited lectures.
Citations (according to Web of Science) > 4000
H-index (according to Web of Science) = 33 (January 2018)

9. Awards:

Copernicus Award for Glorious Study Primus Inter Pares (1974), Gold Cross for Service (1998), Award In Service of Science and the Society (1999), Award of the Commission of National Education (2004), Prizes the Polish Ministry of Science and Higher Education for Outstanding Scientific Achievements of (1999, 2003, 2007, 2011), 'Liebig Lectureship' by German Chemical Society (2012), S. Kostanecki Medal by the Polish Chemical Society (2013), 'Antoni Basinski Lecturship' (Nicolaus Copernicus University, Torun, 2017), J. Žniadecki Medal by the Polish Chemical Society (2018).

10. Family:

Married, spouse: Jadwiga Filarska-Mlosto˝. Children: Anna (1978), Ewa (1980), Katarzyna (1994).

11. Civic activities:

Gardening, travelling, classic music, fine arts.

12. Recent publications:

» Original papers (2013-2017):

  1. A. M. Pieczonka, K. Ciepielowski, Z. Cebulska, G. Mlosto˝, A. Linden, H. Heimgartner
    New Selenocarbazides Derived from Imidazole-Based Carbohydrazides.
    Helv. Chim. Acta, 2013, 96, 397-407.
  2. Korany A. Ali, M.Celeda, G. Mlosto˝, H. Heimgartner,
    Unexpected Reaction Course, of 3-Amino-5-arylopyrazoles with Dialkyl Dicyanfumarates.
    Helv. Chim. Acta, 2013, 96, 633-643.
  3. Emilia Obijalska, Grzegorz Mlosto˝ and Alice Six
    Enantioselective additions of (trifluoromethyl)trimethylsilane to α-iminoketones derived from arylglyoxals.
    Tetrahedron Lett., 2013, 54, 2462-2465.
  4. G. Mlosto˝, E. Obijalska, G. Utecht, H. Heimgartner,
    A new approachto α-(trifluoromethyl)benzyl substituted oxaziridines.
    J. Fluorine Chem., 2013, 151, 7-11.
  5. A. M. Pieczonka, A. Strzelczyk, B. Sadowska, G. Mlosto˝, P. St▒czek,
    Synthesis and Evaluation of Antimicrobial Activity of 3-Oxido-1H-imidazole-4-carbohydrazides Hydrazones.
    Eur. J. Med. Chem., 2013, 64, 389-395.
  6. D. Rygielska-Tokarska, M. Jasi˝ski, G. Mlosto˝, Heinz Heimgartner
    Towards New imidazole-2-thione-based organocatalysts; Sulfur transfer vs. deoxygenation in the reaction of imidazole N-oxides and cycloaliphatic thioketones.
    Phosphprus, Sulfur, and Silicon, 2013, 188, 469-472.
  7. A. Wrˇblewska, G. Mlosto˝
    Synthesis of New enantiopure thiourea derived from (S)-proline.
    Phosphprus, Sulfur, and Silicon, 2013, 188, 509-511.
  8. A. M. Pieczonka, G. Mlosto˝
    Synthesis of enantiopure bis-heterocycles derived from (S)-prolinehydrazide.
    Phosphprus, Sulfur, and Silicon, 2013, 188, 493-495.
  9. A. W. Ivanov, G. Mlosto˝, V. A. Nikolaev,
    Tetrasubstituted oxathiols and olefins from cycloaddition reactions of 2-diazo-1,3-dicarbonyl compounds with aliphatic thiones
    Rusian J. Org. Chem., 2013, 49, 1080-1082.,Zhurnal Organicheskoi Khimii 2013, 49, 1094-1096.
  10. G. Mlosto˝, A. Wrˇblewska, E. Obijalska, H. Heimgartner,
    Optically Active Imidazole N-Oxides Derived from L-Prolinamine.
    Tetrahedron: Asymmetry, 2013, 24, 958-965. (DOI: 10.1016/j.tetasy.2013.07.013).
  11. P. Reisenauer, J. Roma˝ski, G. Mlosto˝, P. R. Schreiner,
    The first matrix isolation oft he methylsulfinyl radical CH3SO.
    Chem. Commun., 2013, 49, 9467-9469. (DOI: 10.1039/c3cc45379k).
  12. G. Mloston, E. Obijalska, P. Ziŕbacz, K. Matyszewski, K. Urbaniak, H. Heimgartner,
    Nucleophilic trifluoromethylation of aziridinyl ketones; a convenient access to fluorinated aziridinyl alcohols.
    J. Fluorine Chem., 2013, 156, 192-197.
  13. V. A. Nikolaev, A. V. Ivanov, L. L. Rodina, G. Mlosto˝,
    Less reactive dipoles of diazodicarbonyl compounds in reactions with cycloaliphatic thioketones; first evidence for the 1,3-oxathiole - thiocarbonyl ylide interconversion
    Beilst. J. Org. Chem., 2013, 9, 2751-2761.
  14. G. Mlosto˝, K. Urbaniak, N. Jacaszek, A. Linden, H. Heimgartner,
    Exploration of fluoral hydrazones derived from carbohydrazides for the synthesis of trifluoromethylated heterocycles.
    Heterocycles, 2014, 88, 387-401. (DOI: 10.3987/COM-13-S(S)40).
  15. A. F. Khlebnikov, A. S. Konev, A. A. Virtsev, D. S. Yufit, G. Mlosto˝, H. Heimgartner,
    Concerted versus Non-Concerted 1,3-Dipolar Cycloadditions of Azomethine Ylides with Electron-Deficient Dialkyl Dicyanobutenedioates.
    Hel. Chim. Acta, 2014, 97, 453-470. (DOI: 10.1002/hlca.201300405)
  16. A. Gebert, M. Jasinski, G. Mloston, H. Heimgartner,
    Unexpected reductions of thioketones with lithium diisopropylamide (LDA)
    Hel. Chim. Acta, 2014, 97, 931-938. (DOI: 10.1002/hlca.201400130)
  17. G. Mlosto˝, E. Obijalska, M. Celeda, V. Mittermeier, A. Linden, H. Heimgartner,
    1,3-Dipolar cycloadditions of fluorinated nitrones with thioketones.
    J. Fluorine Chem., 2014, 165, 27-32 (DOI:org/10.1016/j.jfluchem.2014.05.015).
  18. M. Jasi˝ski, G. Mlosto˝, M. Stolarski, W. Costa, M. Dominguez, H.-U. Reissig,
    Reactions of Cycloaliphatic Thioketones and Their Oxo Analogues with Lithiated Methoxyallene: A New Approach to Vinylthiiranes.
    Chem Asian J., 2014, 9, 2641-2648 (DOI: 10.1002/asia.201402547).
  19. E. Obijalska, M. Kowalski, G. Mlosto˝, A. Linden, H. Heimgartner,
    Chemoselective additions of (trifluoromethyl)trimethylsilane to C=N bonds of α-iminoketones derived from arylglyoxals.
    J. Fluorine Chem., 2014, 168, 151-157. (DOI: org/10.1016/j.jfluchem.2014.09.002)
  20. G. Mlosto˝, K. Urbaniak, K. Gŕbicki, P. Grzelak, H. Heimgartner,
    Hetaryl Thioketones: Synthesis and Selected Reactions.
    Heteroatom Chem., 2014, 25, 548-555. (DOI: 10.1002/hc.21191)
  21. G. Mlosto˝, K. Urbaniak, A. Szychowska, A. Linden, H. Heimgartner,
    Reactions of diphenylketene with aromatic thioketones.
    Heterocycles, 2015, 90, 529-539 (DOI : 10.3987/COM-14-S(K)56)
  22. G. Mlosto˝, P. Pipiak, H. Heimgartner,
    1,3-Dipolar cycloadditions of α-diazoketones derived from N-protected (S)-proline witth aromatic and cycloaliphatic thioketones.
    Helv. Chim. Acta, 2015, 98, 190-200. (DOI: 10.1002/hlca.201400334)
  23. H.-P. Reisenauer, P. R. Schreiner, J. Roma˝ski, G. Mlosto˝,
    Gas-phase generation and matrix isolation of the methylsulfonyl radical CH3SO2.
    J. Phys. Chem., 2015, 119, 2211-2216 (DOI: org/10.1021/jp5036647).
  24. M. Jasi˝ski, G. Mlosto˝, A. Gebert, H. Heimgartner,
    Lithium diisopropylamide (LDA) as an efficient reducing agent for thioketones - mechanistic consideration.
    Phosphorus, Sulfur, and Silicon, 2015, in press.
  25. K. Kowalski, R. Karpowicz, G. Mlosto˝, D. Miesel, A. Hildebrandt, H. Lang, R. Czerwoniec, B. Therrien,
    Synthesis and (spectro)electrochemistry of mixed-valent differrocenyl-dihydrothiopyran derivatives.
    Dalton Transactions, 2015, 44, 6268-6276. (DOI: 10.1039/c5dt00246j)
  26. G. Mlosto˝, K. Urbaniak, A. Linden, H. Heimgartner,
    Selenopen-2-yl substituted thiocarbonyl ylides - at the boarderline of dipolar and diradical reactivity.
    Helv. Chim. Acta, 2015, 98, 453-461. (DOI: 10.1002/hlca.201500050)
  27. A. Wrˇblewska, G, Mlosto˝, H. Heimgartner,
    A new approach to optically active bisheterocycles bearing the N-unsubstituted pyrolidine group.
    Tetrahedron; Asymmetry, 2015, 26, 505-509. (DOI: 10.1016/j.tetasy.2015.03.005)
  28. G. Mlosto˝, P. Pipiak, A. Linden, H. Heimgartner,
    Studies on the reactions of thiocarbonyl S-methanides with hetaryl thioketones.
    Helv. Chim. Acta, 2015, 98, 462-473. (DOI: 10.1002/hlca.201500057)
  29. A. S. Mereshchenko, A. V. Ivanov, V. I. Baranovskii, G. Mloston, L. L. Rodina, V. A. Nikolaev,
    On the strong difference in reactivity of acyclic and cyclic diazodiketones with thioketones: experimental results and quantum-chemical interpretation.
    Beilstein J. Org. Chem. 2015, 11, 504-513 (DOI: 10.3762/bjoc.11.57)
  30. G. Mlosto˝, P. Grzelak, M. Mikina, A. Linden, H. Heimgartner, Hetro-Diels-Alder Reactions of aryl and hetaryl thioketones with acetylenic dipolarophiles.
    Beilstein J. Org. Chem., 2015, 11, 576-582 (DOI:10.3762/bjoc.11.63)
  31. H. P. Reisenauer, J. Roma˝ski, G. Mlosto˝, P. R. Schreiner,
    Reactions of methylsulfinyl radical (CH3(O)S) with oxygen (3O2) in solid argon.
    Chem. Commun., 2015, 10022-10025, (DOI: 10.1039/C5CC02168E)
  32. G. Mlosto˝, A. Wrˇblewska, A. Linden, H. Heimgartner,
    Reactions of (L)-prolinol with aryloglyoxals.
    Asian J. Org., 2015, in press. (DOI: 10.1002/ajoc.201500134R1)
  33. E. Obijalska, G. Utecht, M. K. Kowalski, G. Mlosto˝, M. Rachwalski,
    Nucleophilic additions of (difluoromethyl)trimethylsilane to α-iminoketones and aryl diketones: a new route to the β-amino-α-(difluoromethyl) alcohols.
    Tetrahedron Lett. 2015, 56, 4701-4703. (http://dx.doi.org/10.1016/j.tetlet.2015.06.025)
  34. G. Mlosto˝, A. Wrˇblewska, A. Linden, H. Heimgartner,
    Studies on the reaction of aryl glyoxals with L-prolinol: Unexpected formation of morpholin-2-one derivatives and stereoselective trifluoromethylation of the bicyclic system.
    Asian J. Org. Chem, 2015, 4, 770-777. (DOI: 10.1002/ajoc.201500134R1)
  35. M. Jasi˝ski, G. Mlosto˝, A. Gebert, H. Heimgartner,
    Lithium diisopropylamide (LDA) as an efficient reducing agent for thioketones - mechanistic consideration.
    Phosphorus, Sulfur, and Silicon, 2015, 190, 1281-1284. (DOI: 10.1080/10426507.2015.1012201)
  36. A. Wrˇblewska, G. Mlosto˝, H. Heimgartner,
    Synthesis of optically active polyheterocycles containing pyrrolidine, imidazole, and 1,2,3-triazole rings.
    Tetrahedron; Asymmetry, 2015, 26, 1448-1452. (http://.doi.org/10.1016/j.tetasy.2015.10.019).
  37. G. Mlosto˝, R. Hamera, H. Heimgartner, Synthesis of ferrocenyl thioketones and their reactions with diphenyldiazomethane.
    Phosphorus, Sulfur, and Silicon, 2015, 190, 2125-2133 (http://dx.doi.org/10.1080/10426507.2015.1071817)
  38. G. Mlosto˝, K. Urbaniak, A. Pawlak, H. Heimgartner,
    New application of hetaryl thioketones for the synthesis of hetaryl-substituted ethenes via 'two-fold extrusion reaction'.
    Heterocycles, 2016, 93, ... (DOI : 10.3987/COM-15-S(T)8)
  39. G. Mlosto˝, M. Celeda, H. Heimgartner,
    An unexpected reaction of diethyl phosphite with electron-deficient dialkyl dicyanofumarates.
    Phosphorus, Sulfur, and Silicon, 2016, 191, 207-210, DOI:10.1080/10426507.2015.1085045
  40. G. Mlosto˝, M. Celeda, A. Linden, H. Heimgartner,
    Synthesis of hetaryl-substituted 1,2,4-trithiolanes via three-component reaction with dihetaryl thioketones, benzyl azide and 2,2,4,4-tetramethyl-3-thioxocyclobutanone.
    J. Sulfur Chem., 2016, 37, 14-22 (DOI:org/10.1080/17415993.2015.1082182).
  41. E. Obijalska, A. »urawik, G. Mlosto˝, H. Heimgartner,
    Efficient synthesis of trifluoro- and difluorohydrazides as useful building blocks for fluorinated 1,3,4-oxadiazoles.
    Chem. Heterocycl. Comp., 2016, 52, 133-139 (DOI: DOI 10.1007/s10593-016-1845-3).
  42. G. Mlosto˝, P. Pipiak, H. Heimgartner,
    Diradical reaction mechanisms in [3+2]-cycloadditions of hetaryl thioketones with alkyl- or trimethylsilyl-substituted diazomethanes.
    Beilstein J. Org. Chem., 2016, 12, 716-724 (DOI: 10.3762/bjoc.12.71).
  43. R. Hamera, G. Mlosto˝,
    Ferrocenyl Substituted 1,3-Dithiolanes via [3+2]-Cycloadditions of Thiocarbonyl S-Methanides with Ferrocenyl/Hetaryl Thioketones.
    Phosphorus, Sulfur, and Silicon, 2016, 191, 576-577. (DOI: 10.1080/10426507.2015.1128908).
  44. P. Pipiak, G. Mlosto˝,
    Applications of n-protected (s)-2-(diazoacetyl)pyrrolidine derivatives in the synthesis of optically active nitrogen heterocycles (Heterocycles in Focus),
    Chem. Heterocycl. Comp., 2016, 52, 146-148 (DOI: 10.107/S10593-016-1848-0)
  45. B. Jŕdrzejewska, A. Zakrzewska, G. Mlosto˝, ę. Budzßk, K. Mroczy˝ska, A. M. Grabarz, M. Kaczorowska, D. Jacquemin, B. OÂmia│owski,
    Synthesis and photophysical properties of novel donor-acceptor N-(pyridyn-2-yl) substituted benzo(thio)amides and their difluoroboranyl derivatives.
    Phys. Org. Chem. A, 2016, in press (DOI: 10.1021/acs.jpca.6b04004).
  46. G. Mlosto˝, R. Hamera, A. Linden, H. Heimgartner,
    Synthesis of ferrocenyl-substituted 1,3-dithionaes vis [3+2]-cycloadditions of ferrocenyl hetaryl thioketones with thiocarbonyl S-methanides.
    Beilstein J. Org. Chem., 2016, 12, 1421-1427. (DOI: 10.3762/bjoc.12.136)
  47. G. Mlosto˝, R. Hamera-Fa│dyga, M. Celeda, K. Gŕbicki, H. Heimgartner,
    Synthesis of ferrocenyl- and hetaryl-substituted 2,2,2-trifluoroethanols and their conversion into 2,2,2-trifluoroethanethiols using Lawesson reagent.
    J. Fluorine Chem., 2016, 188, 147-152. (DOI: http://dx.doi.org/10.1016/j.jfluchem.2016.06.017)
  48. G. Mlosto˝, A. Wrˇblewska, H. Heimgartner,
    Synthesis of optically active trifluoromethyl-substituted 2,3-dihydroimidazo[2,1-b]oxazoles.
    J. Fluorine Chem., 2016, 189, 1-6. (DOI: http://dx.doi.org/10.1016/j.jfluchem.2016.07.014)
  49. M. T. Kowalski, G. Mlosto˝, E. Obijalska, A. Linden, H. Heimgartner,
    First application of fluorinated nitrones for the syntehsis of fluoroalkyl β-lactams via Kinugasa.
    Tetrahedron, 2016, 72, 5305-5313. (DOI: 10.1016/j.tet.2016.06.073)
  50. G. Mlosto˝, P. Grzelak, H. Heimgartner,
    Strong influence of the trifluoromethyl group on the chemoselectivity of [3+2]-cycloadditions of thiocarbonyl S-methanides with α,β-unsarurated ketones.
    J. Fluorine Chem., 2016, 190, 56-60. (http://dx.doi.org/doi:10.1016/j.jfluchem.2016.08.009)
  51. A. Michalak, G. Mlosto˝, A. Fruzi˝ski, M. Jasi˝ski,
    Stereoselective 1,3-dipolar cycloadditions of thioketones to carbohydrate-derived nitrones.
    Tetrahedron; Asymmetry, 2016, 27, 973-979. (DOI: org/10.1016/j.tetasy.2016.08.007)
  52. G. Mlosto˝, K. Urbaniak, G. Utecht, D. Lentz, M. Jasi˝ski,
    Trifluoromethylated 2,3-dihydro-1,3,4-thiadiazoles via the regioselective (3+2)-cycloadditions of fluorinated nitrile imines with aryl, hetaryl, and ferrocenyl thioketones.
    J. Fluorine Chem., 2016, 192, 147-154. (DOI: http://dx.doi.org/10.1016/j.jfluchem.2016.10.018)
  53. H. Abul-Futouh, L. R. Almazahreh, , T. Sakamoto, N. Y T. Stessman, D. L. Lichtenberger, R. S. Glass, H. G÷rls, M. El-khateeb, P. Schollhammer, G. Mloston, W. Weigand,
    [FeFe]-Hydrogenase H-Cluster Mimics with Unique Planar μ-(SCH2 )2 ER2 Linkers (E=Ge and Sn).
    Chem. Eur. J., 2016, 22, in press; (DOI: 10.1002/chem.201603843).
  54. J. Hejmanowska, M. Jasi˝ski, G. Mlosto˝, and ú. Albrecht,
    Taming of Thioketones - The First Asymmetric Thio-Diels-Alder Reaction of Thioketones as a Convenient Entry to Optically Active Dihydro-2H-thiopyrans.
    Eur. J. Org. Chem., 2016, in press (DOI: 10.1002/ejoc.201601307)
  55. G. Mlosto˝, P. Grzelak, H. Heimgartner,
    Hetero-Diels-Alder reactions of hetaryl-thiochalcones with acetylenic dienophiles.
    J. Sulfur Chem., 2016, in press (DOI: 10.1080/17415993.2016.1230857)
  56. M. K. Kowalski, G. Mlosto˝, E. Obijalska, H. Heimgartner,
    Application of diethyl ethynephosphonate for the synthesis of 3-phosphonylated β-lactams via Kinugasa reaction.
    Arkivoc, 2017, ii, 59-67. (DOI: http://dx.doi.org/10.3998/ark.5550190.p009.660)
  57. G. Mlosto˝, P. Pipiak, H. Heimgartner,
    [3+2]-Cycloadditions of N-protected '(S)-diazoprolines' with selected acetylenes.
    Heterocycles, 2017, 95, in press (DOI: 10.3987/COM-16-S(S)7)
  58. G. Mlosto˝, K. Urbaniak, A. Pawlak, H. Heimgartner,
    New application of hetaryl thioketones for the synthesis of hetaryl-substituted ethenes via 'two-fold extrusion reaction'.
    Heterocycles, 2017, in press (DOI: 10.3987/COM-15-S(T)8)
  59. G. Mlosto˝, K. Urbaniak, A. Pawlak, H. Heimgartner,
    New application of hetaryl thioketones for the synthesis of hetaryl-substituted ethenes via 'two-fold extrusion reaction'.
    Heterocycles, 2016, 93, 127-139. (DOI: 10.3987/COM-15-S(T)8)
  60. M. K. Kowalski, G. Mlosto˝, E. Obijalska, H. Heimgartner,
    Application of diethyl ethynephosphonate for the synthesis of 3-phosphonylated ?-lactams via Kinugasa reaction.
    Arkivoc, 2017, ii, 59-67. (DOI: http://dx.doi.org/10.3998/ark.5550190.p009.660)
  61. G. Mlosto˝, P. Grzelak, H. Heimgartner,
    Hetero-Diels-Alder reactions of hetaryl-thiochalcones with acetylenic dienophiles.
    J. Sulfur Chem., 2017, 38, 1?10 (DOI: 10.1080/17415993.2016.1230857)
  62. R. Hamera-Fa│dyga, P. Grzelak, P. Pipiak, G. Mlosto˝,
    Microwave assisted synthesis of ferrocenyl and hetaryl functionalized thioketones.
    Phosphorus, Sulfur, Silicon, Relat. Elem. 2017, 192, 197-198. ( DOI: org/10.1080/10426507.2016.1252367).
  63. J. Hejmanowska, M. Jasi˝ski, G. Mlosto˝, ú. Albrecht,
    Taming of thioketones - the first asymmetric thio-diels-alder reaction with thioketones as heterodienophiles.
    Eur. J. Org. Chem., 2017, 950-954 (DOI: 10.1002/ejoc.201601307)
  64. H. Abul-Futouh, L. R. Almazahreh, , T. Sakamoto, N. Y T. Stessman, D. L. Lichtenberger, R. S. Glass, H. G÷rls, M. El-khateeb, P. Schollhammer, G. Mloston, W. Weigand,
    [FeFe]-Hydrogenase H-cluster mimics with unique planar μ-(SCH2 )2 ER2 linkers (E=Ge and Sn).
    Chem. Eur. J., 2017, 23, 346?359 (DOI: 10.1002/chem.201603843).
  65. M. L. McKee, G. Mloston, K. Urbaniak, H. Heimgartner,
    Dimerization reactions of diaryl- and dihetaryl-substituted thiocarbonyl S-methanides as diradical processes - a computational study.
    Beilsten J. Org. Chem., 2017, 13, 410-416 (DOI: doi:10.3762/bjoc.13.44)
  66. G. Mlosto˝, P. Pipiak, H. Heimgartner,
    [3+2]-Cycloadditions of N-protected '(S)-diazoprolines' with selected acetylenes.
    Heterocycles, 2017, 95, 223?231 (DOI: 10.3987/COM-16-S(S)7)
  67. G. Mlosto˝, P. Grzelak, G. Utecht, M. Jasi˝ski.
    First [3+2]-cycloadditions of thiochalcones as C=S dipolarophiles in reactions with fluorinated nitrile imines (Feature Article in Synthesis),
    Synthesis, 2017, 49, 2129-2137 (DOI: 10.1055/s-00000084)
  68. G. Mlosto˝, M. K. Kowalski , E. Obijalska, H. Heimgartner,
    Efficient synthesis of fluoroalkylated 1,4,2-oxathiazoles via regioselective [3+2]-cycloaddition of fluorinated nitrile oxides with thioketones.
    J. Fluorine Chem., 2017, 199, 92-96 (DOI:2org/10.1016/j.jfluchem.2017.04.011)
  69. G. Mloston, R. Hamera-Fa│dyga, H. Heimgartner,
    Unexpected course of the attempted conversion of ferocenyl(hetaryl)methanols into thiols using Lawesson's reagent.
    Phosphorus Sulfur Silcon Relat. Elem., 2017, 192, 732?736. (DOI.org/10.1080/10426507.2017.1286491)
  70. G. Mlosto˝, P. Grzelak, A. Linden, H. Heimgartner,
    Thia-Diels-Alder reactions of hetaryl thioketones with nonactivated 1,3-dienes leading to 3,6-dihydro-2H-pyrans: evidence for a diradical mechanism.
    Chem. Heterocycl. Compd., 2017, 53, 518-525. (http://hgs.osi.lv/index.php/hgs/article/view/3670)
  71. M. K. Kowalski, E. Obijalska,, G. Mlosto˝, H. Heimgartner.
    Generation and reactions of thiocarbonyl S-(2,2,2-trifluoroethanides). Synthesis of trifluoromethylated 1,3-dithiolanes, thiiranes and alkenes.
    J. Fluorine Chem., 2017, 200, 102-108. (DOI: http://dx.doi.org/10.1016/j.jfluchem.2017.06.009)
  72. G. Utecht, J. Sioma, M. Jasi˝ski, G. Mlosto˝,
    Expected and unexpected results in reactions of fluorinated nitrile imines with (cyclo)aliphatic thioketones.
    J. Fluorine Chem., 2017, 201, 68?75. DOI: http://dx.doi.org/doi:10.1016/j.jfluchem.2017.07.014
  73. G. Mlosto˝, P. Pipiak, R. Hamera-Fa│dyga, H. Heimgartner,
    A novel application of silylated 1,3-dithiolanes for the synthesis of aryl-, hetaryl-, and ferrocenyl substituted ethylenes.
    Beilstein J. Org. Chem., 2017, 13, 1900-1906. DOI:10.3762/bjoc.13.185.
  74. G. Mlosto˝, M. Celeda, R. Hamera-Fa│tyga, A. Linden, H. Heimgartner,
    The unusual influence of hetaryl groups on the direct conversion of some secondary alcohols into thiols with Lawesson's reagent: elucidation of the reaction mechanism.
    J. Sulfur Chem., 2017, 38, 475-487 (DOI: 10.1080/17415993.2017.1313257).
  75. G. Mlosto˝, P. Pipiak, J. Voss, D. Buddensiek, A. Senning,
    Generation and selected reactions of chlorinated thiocarbonyl S-imides.
    J. Sulfur Chem., 2017, 38, 530-547 (DOI.org/10.1080/17415993.2017.1325892).
  76. J. Hejmanowska, M. Jasi˝ski, J. Wojciechowski, G. Mlosto˝, ú. Albrecht,
    The first organocatalytic, ortho-regioselective inverse-electron-demand hetero-Diels-Alder reaction.
    Chem. Commun., 2017, 53, 11472-11475 (DOI: 10.1039/C7CC06518C).
  77. K. A. Ali, G. Mlosto˝, K. Urbaniak, A. Linden, H. Heimgartner,
    [3+2]-Cycloadditions of nitrile imines with hetaryl thioketones.
    J. Sulfur, Chem. 2017, 38, 604?613. (DOI: 10.1080/17415993.2017.1346103)
  78. G. Mloston, A. Capperucci, D. Tanini, R. Hamera-Fa│dyga, H. Heimgartner,
    Dialkyl dicyanofumarates as new oxidizing reagents for the converions of thiols into disulfides and selenols into diselenides.
    Eur. J. Org. Chem., 2017, 6831?6839. (DOI: 10.1002/ejoc.201701066)
  79. G. Mlosto˝,
    Heterocycls in materials chemistry.
    Chem. Heterocycl. Comp. 2017, 53, 1-1.

» Review articles:

  1. R. Huisgen, C. Fulka, I. Kalwinsch, L. Xingya, G. Mlosto˝,
    R. Moran, A. Pr÷bstl, Recent developments of the chemistry of thiocarbonyl ylides (a review).
    Bull. Soc. Chim. Belg. 1984, 93, 511-532.
  2. R. Huisgen, E. Langhals, G. Mlosto˝, T. Oshima, J. Rapp,
    New cycloadditions in organic sulfur chemistry.
    Lectures in Heterocycl. Chem., Suppl. of Heterocycl. Chem. 1987, 24S, 1-11.
  3. G. Mlosto˝, J. Roma˝ski, Ch. Schmidt, H.-P. Reisenauer, G. Maier,
    Fotolityczne generowanie reaktywnych ylidˇw tiokarbonylowych w matrycach niskotemperaturowych.
    WiadomoÂci Chem. 1995, 49, 773-776.
  4. L. Fisera, R. Huisgen, I. Kalvinsch, E. Langhals, X. Li, G. Mlosto˝, K. Polborn, J. Rapp, W. Sicking, R. Sustmann,
    New Thione Chemistry.
    J. Pure and Appl. Chem. 1996, 68, 789-798.
  5. G. Mlosto˝, J. Roma˝ski, M. Kńgi, H. Heimgartner,
    Sulfur-Centered Reactive Intermediates; Thiocarbonyl Ylides - Precursors of Some Heterocyclic Compounds.
    Polish J. Appl. Chem., 1997, 41, 361-368.
  6. G. Mlosto˝,
    New Applications of Organic Azides in Syntheses of Sulfur- and Nitrogen-Containing Heterocycles.
    Chem. Papers (Bratislava), 1998, 52, 56-63.
  7. G. Mlosto˝,
    New Adventures with Thioketones and Related Compounds.
    Phosphorus, Sulfur and Silicon, 1999, 153-154, 217-234.
  8. G. Mlosto˝, H. Heimgartner,
    Generation and Typical Reactions of Thiocarbonyl-Ylides (review).
    Polish J. Chem., 2000, 74, 1503-1533.
  9. G. Mlosto˝,
    Reakcje zwi▒zkˇw Siarko-Organicznych z Karbenami oraz Karbenoidami.
    Laboratoria, Aparatura Badania "Lab", 2000 (4), 14-17.
  10. G. Mlosto˝, H. Heimgartner,
    Thiocarbonyl Ylides.
    in Synthetic Applicarions of Dipolar Cycloaddition Chemistry Toward Hetrocycles and Natural Products, Ed. A. Padwa, J.Wiley & Sons, New York 2002 , Chapter 5, 315-360.
  11. G. Mlosto˝,
    Generation of Thiocarbonyl Ylides from 1,3,4-Thiadiazolines - in
    "Nitrogen, Oxygen and Sulfur Ylide Chemistry - Series: Practical Approach in Organic Chemistry", ed. J. S. Clark, Oxford University Press 2002, Chapter 3.12, p. 271-277.
  12. G. Mloston, H. Heimgartner,
    Sulphur-Conatining Heterocycles from Reactions of Thiocarbonyl Compounds with Carbenes and Carbenoids.
    Speciality - Chemicals Magazine, 2003, 23, 38-40.
  13. W. Weigand, S. Braetigam, G. Mlosto˝,
    Selected Cyclic Oligosulfides and Oligosulfide S-Oxides and their Reactions with Platinum(0) Complexes.
    Coordin. Chem. Rev., 2003, 245, 167-175.
  14. H. Heimgartner, G. Mlosto˝,
    2,2,4,4-Tetramethylcyclobutane-1-one-3-thione.
    Electronic Encyclopedia of Reagents for Organic Synthesis, ed. L. A. Paquette, Article - RN 00429, Wiley & Sona, New York 2004.
  15. H. Heimgartner, G. Mlosto˝,
    2,2,4,4-Tetramethylcyclobutane-1,3-dithione.
    Electronic Encyclopedia of Reagents for Organic Synthesis, ed. L. A. Paquette, Article - RN 00430, Wiley and Sons, New York 2004.
  16. R. Huisgen, G. Mlosto˝,
    1,3-Dipolar Cycloadditions - beyond Concertedness (review).
    Modern Problems of Organic Chemistry, 2004, 14, 23-45.
  17. H. Heimgartner, G. Mloston, J. Roma˝ski,
    Adamantanethione.
    Electronic Encyclopedia of Reagents for Organic Synthesis, ed. L. A. Paquette, Article - RN 00504, Wiley & Sons, New York 2005.
  18. J. Roma˝ski, G. Mlosto˝, M. Pietrusiewicz,
    1-Phosphorous-Functionalized 1-(Organosulfanyl)alk-1-enes.
    Sci. Synth. 2005, 24, Section 24.2.14, 541-544.
  19. G. Mlosto˝, H. Heimgartner,
    Synthesis of Sulfur-Heterocycles from aromatic Thioketones. Part I - Three and Four-Membered Rings.
    Targets in Heterocyclic Systems - Chemistry and Properties, Eds. O. A. Attanasi and D. Spinelli, Italian Society of Chemistry, Rome, 2005, 9, 141-157.
  20. G. Mlosto˝, H. Heimgartner,
    Synthesis of Sulfur-Heterocycles from aromatic Thioketones. Part II - Five-, Six- and Seven-Membered Rings.
    Targets in Heterocyclic Systems - Chemistry and Properties, Eds. O. A. Attanasi and D. Spinelli, Italian Society of Chemistry, Rome, 2006, 10, 266-300.
  21. G. Mlosto˝, E. Obijalska, H. Heimgartner,
    Synthesis of β-amino-α-trifluoromethyl alcohols and their application in organic synthesis. (Review)
    J. Fluorine Chem., 2010, 131, 830-844.
  22. G. Mlosto˝, H. Heimgartner,
    Syntheses of Five-membered Sulfur-Heterocycles via 1,5-Dipolar Electrocyclization of Thiocarbonyl Ylides and Related Processes. (Review)
    Current Org. Chem, 2011, 15, 675-693.
  23. G. Mlosto˝, P. R. Schreiner, H. P. Reisenauer, J. Roma˝ski,
    Matrix studies with sulfur heterocycles and related species.
    Phosphorus, Sulfur, Silicon, 2011, 186, 1175-1188.
  24. G. Mlosto˝, E. Obijalska, H. Heimgartner,
    Synthesis of b-amino-a-trifluoromethyl alcohols and their application in organic synthesis. (Review)
    J. Fluorine Chem., 2010, 131, 830-844.
  25. G. Mlosto˝, H. Heimgartner,
    Syntheses of Five-membered Sulfur-Heterocycles via 1,5-Dipolar Electrocyclization of Thiocarbonyl Ylides and Related Processes. (Review)
    Current Org. Chem, 2011, 15, 675-693.
  26. G. Mlosto˝, P. R. Schreiner, H. P. Reisenauer, J. Roma˝ski,
    Matrix studies with sulfur heterocycles and related species.
    Phosphorus, Sulfur, Silicon, 2011, 186, 1175-1188.
  27. G. Mloston, H. Heimgartner,
    2,2-Dimethoxy-5,5-dimethyl-2,5-dihydro-1,3,4-oxadiazol (Review).
    Electronic Encyclopedia of Reagents for Organic Synthesis, ed. L. A. Paquette, Article ľ DOI: 10.1002/047084289X.rn00150, Wiley & Sons, New York 2012.
  28. G. Mlosto˝, H. Heimgartner,
    Sulfur Ylides - Thiocarbonyl Ylides (update 2014).
    Science of Synthesis, 2014, Vol. 27, Chapter 27.1.6.1, pp. 377-384.
  29. G. Mlosto˝, H. Heimgartner,
    Sulfur Ylides - Sulfoxonium Ylides (update 2014).
    Science of Synthesis, 2014, Vol. 27, Chapter 27.1.6.2, pp. 385-392.
  30. G. Mlosto˝, H. Heimgartner,
    Thioaldehyde and Thioketone S-Oxides and S-Imides (Sulfines and Derivatives), Thioketone-S-oxides (update 2014),
    Science of Synthesis, 2014, Vol. 27, Chapter 27.4.3.1, pp. 393-395.
  31. G. Mlosto˝, H. Heimgartner,
    Thioaldehyde and Thioketone S-Oxides and S-Imides (Sulfines and Derivatives), Thioketone-S-imides (update 2014),
    Science of Synthesis, 2014, Vol. 27, Chapter 27.4.3.2, pp. 395-401.
  32. G. Mlosto˝, H. Heimgartner,
    Thioaldehyde and Thioketone S-Sulfides (Thiosulfines),
    Science of Synthesis, 2014, Vol. 27, Chapter 27.26 pp. 403-411.
  33. G. Mlosto˝, H. Heimgartner,
    Sulfur Ylides - Sulfonium Ylides (update 2014).
    Science of Synthesis, 2015, Vol. 27, Chapter 27.1.7, pp. 401-424.
  34. M. Jasi˝ski, A. Wrˇblewska, G. Mlosto˝, and H. Heimgartner,
    Recent progress in the chemistry of 2-unsubstituted imidazole N-oxides.
    Curr. Org. Chem., 2016, 20, 1359-1369 (DOI: 10.2174/1385272820666151210000010).
  35. P. Pipiak, G. Mlosto˝,
    Applications of n-protected (s)-2-(diazoacetyl)pyrrolidine derivatives in the synthesis of optically active nitrogen heterocycles (Heterocycles in Focus)
    Chem. Heterocycl. Comp., 2016, 52, 146-148 (DOI: 10.107/S10593-016-1848-0)
  36. P. Grzelak, G. Mlosto˝,
    Selected applications of thiobenzophenone for the syntheses of 3-, 4-, 5- and 6-membered sulfur heterocycles (Heterocycles in Focus)
    Chem. Heterocyclic Comp., 2016, 52, 282-284. (DOI: 10.1007/s10593-016-1878-7)
  37. G. Mlosto˝, P. Grzelak, R. Hamera-Fa│tyga, M. Jasi˝ski, P. Pipiak, ú. Albrecht, J. Hejmanowska, H. Heimgartner,
    Aryl, Hetaryl, and Ferrocenyl Thioketones as Versatile Building Blocks for Exploration in the Organic Chemistry of Sulfur
    Phosphorus, Sulfur, and Silicon, 2016, in press, (DOI: org/10.1080/10426507.2016.1252368).
  38. G. Mlosto˝, P. Grzelak, R. Hamera-Fa│tyga, M. Jasi˝ski, P. Pipiak, ú. Albrecht, J. Hejmanowska, H. Heimgartner,
    (procecdings after ISOCS-27th)
  39. Aryl, hetaryl, and ferrocenyl thioketones as versatile building blocks for exploration in the organic chemistry of sulfur.
    Phosphorus, Sulfur, Silicon, Relat. Elem. 2017, 192, 204-211 (DOI: org/10.1080/10426507.2016.1252368).
  40. G. Mlosto˝, H. Heimgartner,
    Dialkyl dicyanofumarates and dicyanomaleates as versatile building blocks for synthetic organic chemistry and mechanistic studies
    Beilstein J. Org. Chem., 2017, 13, 2235-2251. (DOI: 10.3762/bjoc.13.221)