93. ---- M. Canton, M. Thierry, F. Larras, P. Bicherel, L. Mata, N. Delpit, A. Lapczynski, P. Thomas, S. Antoniotti. Chemical composition of volatile and non-volatile fractions of galbanum (Ferula galbaniflua Boiss.) resinoid en route to ecotoxicity assessment.

92. ---- H. Birch, K. Scharling Dyhr, S. Antoniotti, M. Thierry, A. Lapczynski, P. Mayer. Whole UVCB tests can yield biotic and abiotic degradation kinetics of known and unknown constituents for an enhanced UVCB degradation profile.

91. ---- T. Puzyn, J. Polanski, S. Antoniotti, J.-B. Coffin, S. Fiorucci, A. Racz, A. Mikolajczyk, P. Skurski, K. Polański, U. Zhdan. From scaffold-based libraries to data-driven generative and chemogenomic models. 

90. ---- M. Thierry, M. Himbaut, A. Roch, C. Laudamiel, S. Antoniotti. L’extraordinaire histoire d’un flacon de parfum.

89. ---- M. Pierson, S. Antoniotti. Subtraction of chromatograms for an easy and automatible detection of conformity and adulteration issues.

88. ---- M. Pierson, X. Fernandez, S. Antoniotti. Meta-analysis of published chemical compositions of Mentha sp. essential oils and tentative estimation of the phenomenon of natural variation.

87. ---- S. Antoniotti. Informer pour agir : la diplomatie scientifique au cœur des COP. Expressions, Institut Montaigne, 2024, 24/01. Montaigne.

86. ---- K. Plevova, V. Michelet, S. Antoniotti. Emulation of Transition Metal-based Catalytic Systems by Small Gold Nanoparticles. Tandem Cyclisation/Reduction and Cyclisation/Hydroalkoxylation Reactions with Improved Scalability.

85. ---- M. Canton, M. Thierry, S. Antoniotti. Chemical and olfactory analysis of essential oils of Hedychium gardnerianum, Hedychium flavescens, Pittosporum senacia, Psidium cattleianum from Reunion French Island. J. Essent. Oil Plant Comp2023, 1(3), 298-311. Current Science Publishing (OPEN ACCESS). HAL.

84. ---- M. Lecourt, S. Antoniotti. Biocatalysis & biotransformation for optimised natural flavour and fragrance ingredients. Book chapter, sous presse.

83. ---- M. Pierson, S. Antoniotti. Modern or renewed techniques and approaches for the detection of adulteration of essential oils. Book chapter, sous presse.

82. ---- E. Tempio, A. Ravez, D. Lach, M. Kapkowski, K. Plevova, L. Gilles, J. Polanski, S. Antoniotti. Iron(III) Chloride-catalysed acetalisation of α,β-unsaturated carbonyl compounds towards odorant ketals. Tetrahedron 2023, 149, 133734. ElsevierHAL.

81. ---- M. Himbaut, C. Dubois, S. Antoniotti, X. Fernandez. Actifs cosmétiques antichute de cheveux et activateurs de croissance. Tech. Ing., 2023, J3010, Techniques de l'ingénieur.

80. ---- L. Gilles, S. Antoniotti. Chemical and olfactory analysis of the volatile fraction of Ocimum gratissimum concrete from Madagascar. Chem. Biodiv. 2023, e202300252. Wiley (OPEN ACCESS). HAL.

79. ---- A. Mikolajczyk, U. Zhdan, S. Antoniotti, A. Smolinski, K. Jagiello, P. Skurski, M. Harb, T. Puzyn, J. Polanski. Retrosynthesis from transforms to predictive sustainable chemistry and nanotechnology: a brief tutorial review. Green Chem., 2023, 25, 2971-2991. RSC. HAL.

78. --- M. Lecourt, G. Chietera, B. Blerot, F. Jullien, S. Antoniotti. From biosynthesis in plants to post-biosynthetic enzymatic conversion. Generation of odor-impact rose oxides from citronellol-rich essential oils. Botany Lett., 2023, 70, 1, 15-27. Taylor & Francis. HAL.

77. ---- L. Gilles, S. Antoniotti. Spirocyclic compounds in fragrance chemistry: synthesis and olfactory properties. ChemPlusChem, 2022, 87, 11. e202200227. Wiley (OPEN ACCESS). HAL.

76. ---- M. Lecourt, C. Giorgiana, B. Blerot, S. Antoniotti. Laccase-catalyzed oxidation of allylbenzene derivatives: towards a green equivalent of ozonolysis. Molecules, 2021, 26, 19, 6053. MDPI (OPEN ACCESS). HAL.

75. ---- M. Lecourt, S. Antoniotti. Les biotechnologies blanches au service de la parfumerie et les nouveaux ingrédients biotech. Nez, La revue 2021, Nez. HAL.

74. ---- M. Pierson, X. Fernandez, S. Antoniotti. Type and magnitude of cases of non-compliance and adulteration in neroli, mandarin and bergamot essential oils purchased on-line and vulnerability of end-users. Sci. Rep. 2021, 11, Article number: 11096. Nature (OPEN ACCESS). HAL.

73. ---- M. Lecourt, S. Antoniotti. Chemistry, sustainability and naturality of perfumery biotech ingredients. ChemSusChem, 2021, 13, 21, 5600-5610. Wiley. HAL.

cover chemsuschem Mathilde
cover chemsuschem Mathilde

72. ---- L. Gilles, S. Antoniotti. Chimie durable et parfumerie. Nez, La revue 2020, NEZ. HAL.

71. ---- T. Siudyga, M. Kapkowski, P. Bartczak, M. Zubko, J. Szade, K. Balin, S. Antoniotti, J. Polanski. Ultra-low temperature carbon (di)oxide hydrogenation catalyzed by hybrid ruthenium-nickel nanocatalysts: towards sustainable methane production. Green Chem202022, 5143-5150. RSC. HAL.

70. ---- H. Bouges, A. Monchot, S. Antoniotti. Enzyme-catalysed conversion of atranol and derivatives into dimeric hydrosoluble materials. Application to the preparation of a low-atranol oakmoss absolute. Cosmetics 2018, 5(4), 69. MDPI (OPEN ACCESS). HAL.

69. ---- H. Bouges, K. Calabro, O. P. Thomas, S. Antoniotti. Unusual polycyclic fused product by oxidative enzymatic dimerisation of 5-methylpyrogallol catalyzed by horseradish peroxidase/H2O2. Molecules 2018, 23(10), 2619MDPI (OPEN ACCESS). HAL.


68. ---- N. Elizarov, P. D. Giorgi, A. Yeromina, S. Antoniotti. Complex molecules synthesis made easy. Proceedings of the 1st UCA days 2018HAL (OPEN ACCESS).

67. ---- P. D. Giorgi, V. Liautard, M. Pucheault, S. Antoniotti. Biomimetic Cannabinoid Synthesis Revisited: Batch and Flow All‐Catalytic Synthesis of (±)‐ortho‐Tetrahydrocannabinols and Analogues from Natural Feedstocks. Eur. J. Org. Chem201811, 1307-1311. Cover picture. Wiley. HAL.

66. ---- P. D. Giorgi, S. Antoniotti. Catalytic tandem reactions triggered by the introduction of a carbonyl function. Advances in Organic Synthesis, Ed. Atta-ur-Rahman, 2018, 8, 1-31 (Invitation). Bentham Science. HAL.

65. ---- X. Fernandez, S. Antoniotti, J. Golebiowski. Ingrédients odorants et design olfactif. In: La chimie et les sens, 2018, Dunod (Paris). EDP Sciences

64. ---- S. Antoniotti, J.-G. Boiteau. Réactifs nucléophiles organométalliques en synthèse organique. Théorie et applications. Tech. Ing2018, AF6511. Techniques de l'ingénieur.

63. ---- P. D. Giorgi, S.-H. Soo-Tang, S. Antoniotti, J. C. van der Waal. Catalytic oxidation of biosourced 3-methylphtalic anhydride under O2: one-pot hemimellitic acid synthesis and novel example of biomass valorization. ChemistrySelect2017 , 2, 33, 10766–10770. Wiley. HAL.

62. ---- B. Touati, A. El Bouakher, M. Salah Azizi, C. Taillier, R. Ben Othman, M. Trabelsi-Ayadi, S. Antoniotti, E. Duñach, V. Dalla. Atom-economic catalytic direct substitution of N,O-acetals with simple ketones. Eur. J. Org. Chem2017, 30, 4445-4460. Wiley. HAL.

61. ---- I. Notar Francesco, J.-J. Filippi, S. Antoniotti. Sustainable manufacture of a valuable fragrance ingredient: Lipase-catalysed acylation of vetiver essential oil and chemoselectivity between sesquiterpene alcohols. ChemPlusChem201782, 3, 407-415. Wiley. Highlighted in the Wiley Hot topics : biocatalysis. HAL.

60. ---- H. Bouges, S. Antoniotti. Synthesis of deuterated methyleugenol via transition metal-catalysed coupling of substituted deuterated benzyl chloride with vinylmagnesium bromide. Flavour Fragr. J., 201732, 3, 191-195. Wiley

59. ---- P. D. Giorgi, N. Elizarov, S. Antoniotti. Selective oxidation of activated alcohols by supported gold nanoparticles under an atmospheric pressure of O2: batch and continuous flow studies. ChemCatChem 2017, 9, 10, 1830-1836. Wiley. Highlighted by Wiley in Hot topics : gold. HAL.

58. ---- P. D. Giorgi, P. J. Miedziak, J. K. Edwards, G. J. Hutchings, S. Antoniotti. Bicatalytic multistep reactions en route to the one-pot total synthesis of complex molecules: easy access to chromene and 1,2-dihydroquinoline derivatives from simple substrates. ChemCatChem 2017, 9, 1, 70-75. Wiley. Cover picture. Highlighted by Wiley in Hot topics : sustainable chemistry. HAL.


57. ---- N. Elizarov, M. Pucheault, S. Antoniotti. Highly efficient Hosomi-Sakurai reaction of aromatic aldehydes catalyzed by Montmorillonite doped with simple bismuth(III) salts. Batch and continuous flow studies. ChemistrySelect 20161, 12, 3219-3222. Wiley

56. ---- S. Antoniotti. Catalyse par des nanoparticules métalliques. Tech. Ing2016, AF6508. Techniques de l’ingénieur.

55. ---- X. Fernandez, S. Antoniotti. Parfums : matières premières, formulations et applications. Tech. Ing2016, J2304. Techniques de l’ingénieur.

54. ---- L. Laurençon, T. K. T. Do, F. Hadji-Minaglou, S. Antoniotti, X. Fernandez. Fast and efficient chromatographic methods for quantification of total saponins in Solidago virgaurea L. ssp. extracts. Comparison of high pressure liquid chromatography and high performance thin-layer chromatography. J. Planar Chrom201629, 6, 410–416. Springer.

53. ---- B. Touati, A. El Bouakher, C. Taillier, R. Ben Othman, M. Trabelsi-Ayadi, S. Antoniotti, E. Dunach, V. Dalla. Enolizable carbonyls and N,O-acetals: A rational approach for room-temperature Lewis superacid-catalyzed direct α-amidoalkylation of ketones and aldehydes. Chem. Eur. J. 201622, 17, 6012–6022. Wiley. HAL.

52. ---- I. Notar Francesco, B. Cacciuttolo, O. Pascu, C. Aymonier, M. Pucheault, S. Antoniotti. Simple salts of abundant metals (Fe, Bi, and Ti) supported on Montmorillonite as efficient and recyclable catalysts for regioselective intramolecular and intermolecular hydroalkoxylation reactions of double bonds and tandem processes. RSC Advances20166, 19807 - 19818. RSC

51. ---- I. Notar Francesco, B. Cacciuttolo, M. Pucheault, S. Antoniotti. Simple metal salts supported on Montmorillonite as recyclable catalysts for intramolecular hydroalkoxylation of double bonds in conventional and VOC exempt solvents. Green Chem201517 , 2, 837 - 841. RSC

50. ---- T. K. T. Do, F. Hadji-Minaglou, S. Antoniotti, X. Fernandez. Essential oil authenticity: a challenge for the analytical chemist. Trends Anal. Chem. 201566, 146–157. Elsevier

49. ---- I. Notar Francesco, J. Giauffret, F. Fontaine-Vive, J. K. Edwards, C. J. Kiely, G. J. Hutchings, S. Antoniotti. Novel radical tandem 1,6-enynes thioacylation / cyclisation: Au-Pd nanoparticles catalysis versus thermal activation as a function of the substrate specificity. Tetrahedron 201470, 51, 9635–9643. Elsevier

48.---- S. Antoniotti. Tuning of essential oils properties by enzymatic treatment: Towards sustainable processes for the generation of new fragrant ingredients. Molecules 201419, 7, 9203-9214. (Invitation) OPEN ACCESS

47. ---- I. Notar Francesco, F. Fontaine-Vive, S. Antoniotti. Synergies in the catalytic activity of bimetallic nanoparticles and new synthetic methods for the preparation of fine chemicals. ChemCatChem 20146, 10, 2784-2791. Lien

46. ---- K. Ben Hadj Hassen, K. Gaubert, M. Vaultier, M. Pucheault, S. Antoniotti. Comparison of homogeneous and heterogeneous Ga(III)-catalysis in the cycloisomerisation of 1,6-enynes. Green Chem. Lett. Rev. 20147, 3, 243-249. OPEN ACCESS

45. ---- T. K. T. Do, F. Hadji-Minaglou, S. Antoniotti, X. Fernandez. Secondary metabolites isolation in natural products chemistry: comparison of two semipreparative chromatographic techniques (HPLC and HPTLC). J. Chrom. A 20141325, 256–260. Lien

44. ---- P. Nava, Y. Carissan, J. Drujon, F. Grau, J. Godeau, S. Antoniotti, E. Duñach, S. Humbel. Theoretical study of the catalysis of the cycloisomerisation of 1,6-dienes with Sn(IV) salts: important role of a water molecule. ChemCatChem 20146, 2, 500-507. Lien. Inside cover.

43. ---- J. Ramilijaona, E. Raynaud, C. Bouhlel, E. Sarrazin, X. Fernandez, S. Antoniotti. Enzymatic modification of palmarosa essential oil: chemical analysis and olfactory evaluation of acylated products. Chem. Biodiv201310, 12, 2291–2301. Lien

42. ---- J. Godeau, F. Grau, S. Antoniotti, E. Duñach. Preparation and olfactory evaluation of mono- and bicyclic compounds featuring gem-dimethylcyclohexane structures. Flavour Fragr. J201329, 1, 59–66. Lien

41. ---- R. Belaqziz, F. Bahri, A. Romane, S. Antoniotti, X. Fernandez, E. Duñach. Essential oil composition and antibacterial activity of the different parts of Thymus maroccanus Ball: an endemic species in Morocco(†). Nat. Prod. Res201327, 18, 1700-1704. Lien

40. ---- S. Antoniotti. Chimie verte - Chimie durable. Ellipses (Paris) 2013, pp 192. Lien.


39. ---- S. Antoniotti, M. Abert Vian, F. Chemat. Les huiles essentielles comme ingrédients pour une chimie « verte ». In : Fernandez, Chemat (Eds) : La chimie des huiles essentielles, 2012, Vuibert (Paris). Lien

38. ---- J. Godeau, F. Fontaine-Vive, S. Antoniotti, E. Duñach. Experimental and theoretical studies of the bismuth triflate-catalysed cycloisomerisation reaction of 1,6,10-trienes and aryl polyenes. Chem. Eur. J.201218, 52, 16815-16822. Lien.

37. ---- V. Vece, K. Ben Hadj Hassen, S. Antoniotti, E. Duñach. C-O and C-C bonds formation in the cyclisation of gem-(dialkoxymethyl)-1,6-dienes catalysed by tin(IV) triflimidate at room temperature. Tetrahedron Lett201253, 38, 5102-5105. Lien. Abstracted in Cheminform

36. ---- C. Bouhlel, G.’A. Dolhem, X. Fernandez, S. Antoniotti. Model study of the enzymatic modification of natural extracts: peroxidase-based removal of eugenol from rose essential oil. J. Agric. Food Chem201260, 4, 1052-1058. Lien

35. ---- A.-L. Groussin, S. Antoniotti. Valuable chemicals by the enzymatic modification of molecules of natural origin: terpenoids, steroids, phenolics and related compounds. Bioresource Technol2012115, 237-243. Lien

34. ---- O. Thomas, S. Antoniotti. Exercices et QCM de chimie organique UE1. Collection PACES, 2011, Ellipses (Paris). Lien

33. ---- O. Thomas, S. Antoniotti. Cours de chimie organique UE1. Collection PACES, 2011, Ellipses (Paris). Lien

32. ---- G. Genta-Jouve, S. Antoniotti, O. P. Thomas. Polyketide assembly mimics and biomimetic access to aromatic rings. In : Poupon, Nay (Eds) : Biomimetic Organic Synthesis, 2 Vol., 2011, Wiley-VCH Verlag (Weinheim). Lien vers le site de Wiley. Abstracted in Cheminform

Highlighted in Angew. Chem. Int. Ed201251, 583. Lien

31. ---- J. Godeau, S. Olivero, S. Antoniotti, E. Duñach. Biomimetic cationic polyannulation reaction catalyzed by Bi(OTf)3: cyclization of 1,6-dienes, 1,6,10-trienes and aryl trienes. Org. Lett201113, 13, 3320-3323. Lien. Highlighted in Methods in Organic Synthesis abstracts and in Catalysts and Catalysed Reactions abstracts. Abstracted in Cheminform

30. ---- S. Antoniotti, S. Poulain-Martini, E. Duñach. Electrophilic functionalization of non-activated olefins catalyzed by Lewis superacids. Synlett 2010, 2973-2988. Lien. Abstracted in Cheminform

29. ---- S. Antoniotti, V. Dalla, E. Duñach. Metal Triflimidates : better than Metal Triflates as Catalysts in Organic Synthesis-the Effect of a Highly Delocalised Counter-Anion. Angew. Chem. Int. Ed201049, 43, 860-7888. Lien. Highlighted in Catalysts and Catalysed Reactions abstracts and in Methods in Organic Synthesis abstracts. Abstracted in Cheminform.

28. ---- R.-M. Dia, R. Belaqziz, A. Romane, S. Antoniotti, E. Duñach. Flavouring and odorant thiols from renewable resources by InIII-catalysed hydrothioacetylation and lipase-catalysed solvolysis. Tetrahedron Lett201051, 16, 2164-2167. Lien. Abstracted in Cheminform

27. ---- R. Ben Othman, R. Affani, M.-J. Tranchant, S. Antoniotti, V. Dalla, E. Duñach. N-Acyliminium ions chemistry : highly efficient and versatile carbon-carbon bond formation by nucleophilic substitution of hydroxyl groups catalyzed by Sn(NTf2)4. Angew. Chem. Int. Ed201049, 776-780. HOT PAPER. Lien. Highlighted in Catalysts and Catalysed Reactions abstracts and in Methods in Organic Synthesis abstracts. Abstracted in Cheminform.

26. -----S. Antoniotti, E. Duñach. Tin(IV) triflimidate-catalyzed cyclization of epoxy esters to functionalized δ-hydroxy-γ-lactones. Tetrahedron Lett200950, 21, 2536-2539. Lien. Highlighted in Methods in Organic Synthesis abstracts. Abstracted in Cheminform

25. -----S. Antoniotti. 4th French-Italian Chemistry Congress : Environment and Sustainable Development. C. R. Chim200912, 8, 829-830. Lien

24. -----J. Godeau, S. Olivero, S. Antoniotti, E. Duñach. Lewis superacids derived from triflic and triflimidic acids and their use as catalysts in 1,6-dienes cycloisomerisation. C. R. Chim. 200912, 8, 911-915 . Lien

23. -----X. Fernandez, S. Antoniotti, E. Bussotti, M.-P. Hurel. Parfum, chimie et création. Actual. Chim2008, 323-324, 42-51. Lien.

22. -----P. Y. Toullec, E. Genin, S. Antoniotti, J.-P. Genêt, V. Michelet. Au2O3 as a highly stable and efficient catalyst for the selective cycloisomerisation of -acetylenic carboxylic acids to -alkylidene -butyrolactones. Synlett 2008, 707-711. Lien. Highlighted in the Organic Chemistry Portal, in Catalysts and Catalysed Reactions abstracts and in Methods in Organic Synthesis abstracts. Abstracted in Cheminform

21. -----S. Antoniotti, X. Fernandez, E. Duñach. Substrate scope evaluation of hydrolases and enzymatic reaction design. Biocatal. Biotransfor200826, 3, 228-234. Lien

20. -----S. Antoniotti, E. Duñach. Facile preparation of metallic triflates and triflimidates by oxidative dissolution of metal powders. Chem. Comm2008, 993-995. Lien

19. -----P. Lemechko, F. Grau, S. Antoniotti, E. Duñach. Hydroalkoxylation of non-activated olefins catalysed by Lewis superacids in alcoholic solvents : An eco-friendly reaction. Tetrahedron Lett. 200748, 5731-5734. Lien. Abstracted in Cheminform

L’introduction de cet article a été plagiée dans un article paru 2 ans plus tard. Plagiarism of the introduction of his article occured 2 years after in : Tetrahedron Letters, 2009, 50, 5783-5785. Lien

18. -----F. Berrué, S. Antoniotti, O. Thomas, P. Amade. Bioinspired metal-catalysed Doebner - Knoevenagel condensations between malonic acid half thioesters and aldehydes. Eur. J. Org. Chem. 200711, 1743-1748 . Lien. Highlighted in Catalysts and Catalysed Reactions abstracts. Abstracted in Cheminform

17. -----E. Genin, P. Y. Toullec, P. Marie, S. Antoniotti, C. Brancour, J.-P. Genêt, V. Michelet. Gold catalysis in organic synthesis : efficient intramolecular cyclization of gamma-acetylenic carboxylic acids to 5-exo-alkylidene-butyrolactones. ARKIVOC 2007V, 67-78. Lien

16. -----R. F. Klees, P. C. De Marco, R. M. Salasznyk, D. Ahuja, M. G. Hogg, S. Antoniotti, L. Kamath, J. S. Dordick, G. E. Plopper. Apocynin derivatives interrupt intracellular signalling resulting in decreased migration in breast cancer cell.  J. Biomed. Biotechnol. 2006, 1-10. Lien

15. -----S. Antoniotti, J. Golebiowski, D. Cabrol-Bass, E. Duñach. Density Functional Theory investigations on acid-catalysed epoxide oxidative ring-opening by DMSO. Competition between oxidation processes. J. Mol. Struct. (Theochem) 2006763, 155-9. Lien

14. ------E. Genin, P. Y. Toullec, S. Antoniotti, C. Brancour, J.-P. Genêt, V. Michelet. Room Temperature Au(I)-Catalyzed exo-Selective Cycloisomerization of Acetylenic Acids : An Entry to Functionalized -Lactones. J. Am. Chem. Soc2006128, 3112-3113. Lien. Highlighted in the Organic Chemistry Portal. Abstracted in Cheminform

*** Ranked in the JACS most-cited articles in 2006 *** 

as of December 31, 2006 (#13) 

as of December 31, 2007 (#20) 

13. ------E. Genin, S. Antoniotti, V. Michelet, J.-P. Genêt. An Ir(I)-catalyzed exo-selective tandem cycloisomerization / hydroalkoxylation of bis-homopropargylic alcohols at room temperature. Angew. Chem. Int. Ed. 200544, 4949-53. Lien. Highlighted in Catalysts and Catalysed Reactions abstracts. Abstracted in Cheminform

12. ------S. Antoniotti, E. Genin, V. Michelet, J.-P. Genêt. Highly efficient access to strained bicyclic ketals via gold-catalyzed cycloisomerization of bis-homopropargylic diols. J. Am. Chem. Soc2005127, 9976-9977. Lien. Highlighted in Methods in Organic Synthesis abstracts. Abstracted in Cheminform

11. ------S. Antoniotti, J. S. Dordick. Peroxidase-catalyzed coupling of solid-supported ortho-methoxyphenols. Adv. Synth. Catal. 2005347, 1119-24. Lien

10. ------S. Antoniotti, S. Antonczak, J. Golebiowski. Acid-catalysed oxidative ring-opening of epoxide by DMSO. Theoretical investigation of the effect of acid catalysts and substituents. Theor. Chem. Acc. 2004112, 290-7. Lien

9. ------S. Antoniotti, E. Duñach. Mechanistic aspects of the Bi-catalysed oxidation of epoxides to -diketones. Eur. J. Org. Chem. 2004, 3459-64. Lien. Highlighted in Catalysts and Catalysed Reactions abstracts

8. ------S. Antoniotti, E. Duñach. Utilisations récentes de dérivés du bismuth en synthèse organique. Comptes Rendus Chimie 20047, 679-88. Lien. Abstracted in Cheminform

7. ------S. Antoniotti, N. Alezra, X. Fernandez, E. Duñach. Catalytic epoxide oxidation : a novel access to various flavouring and odorant -diketones. Flavour Frag. J. 200419, 373-81. Lien. Highlighted in Methods in Organic Synthesis abstracts

6. ------S. Antoniotti, L. Santhanam, D. Ahuja, M. G. Hogg, J. S. Dordick. Structural diversity of peroxidase-catalyzed oxidation products of ortho-methoxyphenols. Org. Lett. 20046, 1975-8. Lien

5. ------S. Antoniotti, E. Duñach. Studies on the catalytic oxidation of epoxides to alpha-diketones by Bi(0)/O2 in DMSO. J. Mol. Catal. A 2004208, 135-45. Lien

4. ------S. Antoniotti, E. Duñach. Epoxide oxidations : a valuable tool in organic synthesis. Synthesis 2003, 2753-62. Lien. Highlighted in Methods in Organic Synthesis abstracts. Abstracted in Cheminform

3. ------S. Antoniotti. Bismuth(III) trifluoromethanesulfonate. Synlett 2003, 1566-7. Lien. *** Ranked in the 5 most cited Synlett spotlights over 10 years (see here). *** 

2. ------S. Antoniotti, E. Duñach. Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines. Tetrahedron Lett200243, 3971-3. Lien. Highlighted in Methods in Organic Synthesis abstracts. Abstracted in Cheminform

1. ------S. Antoniotti, E. Duñach. Novel and catalytic oxidation of internal epoxides to -diketones. Chem. Commun. 2001, 2566-7. Lien. Abstracted in Cheminform.