Publications of the last 5 years

Here is a list of publications of the team over the last 5 years, for all the data you can view the output page.

Refereed articles (rank A)

  1. Domingues, M. ; Jaszczyk, J. ; Ismael, M. I. ; Figueiredo, J. A. ; Daniellou, R. ; Lafite, P. ; Schuler, M. ; Tatibouët, A.
    Conformationally restric ted oxazolidin-2-one fused bicyclic iminosugars as potential glycosidase inhibitors
    Eur. J. Org. Chem. 2020, 6109-6126.
    Impact Factor: 2.889

  2. Zarafu, I. ; Matei, L. ; Bleotu, C. ; Ionita, P. ; Tatibouët, A. ; Păun, A. ; Nicolau, I. ; Hanganu, A. ; Limban, C. ; Nuta, D. C. ; Nemeș, R. M. ; Diaconu, C. C. ; Radulescu, C.
    Synthesis, characterization, and biologic activity of new acyl hydrazides and 1,3,4-oxadiazole derivatives
    Molecules 2020, 25, 3308.
    Impact Factor: 3.267

  3. Claude, B. ; Cutolo, G. ; Farhat, A. ; Zarafu, I. ; Ionita, P. ; Schuler, M. ; Tatibouët, A. ; Morin, Ph. ; Nehmé, R.
    Capillary electrophoresis with dual detection UV/C4D for monitoring myrosinase-mediated hydrolysis of thiol glucosinolate designed for gold nanoparticle conjugation
    Anal. Chim. Acta 2019, 1085, 117-125.
    Impact Factor: 5.256

  4. Fredy, J. W. ; Hubert-Roux, M. ; Sabot, C. ; Renard, P.-Y. ; Cutolo, G. ; Nehmé, R. ; Schuler, M. ; Tatibouët, A. ; Poret, B. ; Gandolfo, P. ; Castel, H.
    Diverted natural lossen-type rearrangement for bioconjugation through in situ myrosinase-triggered isothiocyanate synthesis
    Bioconjugate Chem. 2019, 30, 1385–1394.
    Impact Factor: 4.349

  5. Lafite, P. ; Marroun, S. ; Coadou, G. ; Montaut, S. ; Marques, S. ; Schuler, M. ; Rollin, P. ; Tatibouët, A. ; Daniellou, R. ; Oulyadi, H.
    S-glycosyltransferase UGT74B1 can glycosylate both S- and O-acceptors: mechanistic insights through substrate specificity
    Molecular Catalysis 2019, 479, 110631.
    Impact Factor: 2.938

  6. Cutolo, G. ; Reise, F. ; Schuler, M. ; Nehmé, R. ; Despras, G. ; Brekalo, J. ; Morin, Ph. ; Renard, P.-Y. ; Lindhorst, T. K. ; Tatibouët, A.
    Bifunctional mannoside-glucosinolate glycoconjugates as enzymatically triggered isothiocyanates and FimH ligands
    Org. Biomol. Chem. 2018, 16, 4900 - 4913.
    Impact Factor: 3.49

  7. Legros, V. ; Taing. G. ; Buisson, P. ; Schuler, M. ; Bostyn, S. ; Rousseau, J. ; Sinturel, C. ; Tatibouët, A.
    Activated glycerol carbonates, versatile reagents with aliphatic amines: formation and reactivity of glycidyl carbamates and trialkylamines
    Eur. J. Org. Chem. 2017, 5032-5043.
    Impact Factor: 2.882

  8. Marzag, H. ; Schuler, M. ; Tatibouët, A. ; Reboul, V.
    Synthesis of methionine-derived endocyclic sulfilimines and sulfoximines
    Eur. J. Org. Chem. 2017, 896-900.
    Impact Factor: 2.834

  9. Da Costa, P. L. ; Melo, V. N. ; Guimaraes, B. M. ; Schuler, M. ; Pimenta, V. ; Rollin, P. ; Tatibouët, A. ; De Oliveira, R. N.
    Glycerol carbonate in Ferrier reaction: Access to new enantiopure building blocks to develop glycoglycerolipid analogues
    Carbohydr. Res. 2016, 436, 1-10.
    Impact Factor: 2.096

  10. Marroun, S. ; Montaut, S. ; Marques, S. ; Lafite, P. ; Coadou, G. ; Rollin, P. ; Jousset, G. ; Schuler, M. ; Tatibouët, A. ; Oulyadi, H. ; Daniellou, R.
    UGT74B1 from Arabidopsis thaliana as a versatile biocatalyst for the synthesis of desulfoglycosinolates
    Org. Biomol. Chem. 2016, 14, 6252-6261.
    Impact Factor: 3.564

  11. Chéry, F. ; Cabianca, E. ; Tatibouët, A. ; De Lucchi, O. ; Lindhorst, T. K. ; Rollin, P.
    Reductive opening of carbohydrate phenylsulfonylethylidene (PSE) acetals
    Carbohydr. Res. 2015, 417, 117-124.
    Impact Factor: 1.817

  12. Marquès, S. ; Schuler, M. ; Tatibouët, A.
    Preparation of pyranose-based thioimidate N-oxides (TINOs
    Eur. J. Org. Chem. 2015, 2411-2427.
    Impact Factor: 3.15

  13. Matei, L. ; Bleotu, C. ; Baciu, I. ; Diaconu, C. C. ; Hanganu, A. ; Banu, O. ; Ionita, P. ; Paun, A. ; Tatibouët, A. ; Zarafu, I.
    Synthesis and biological activities of some new isonicotinic acid 2-(2-hydroxy-8-substituted-tricyclo[7.3.1.02.7)]tridec-13-ylidene)-hydrazides
    Bioorg. Med. Chem. 2015, 23, 401-410.
    Impact Factor: 2.951

the average impact factor is : 3.191



Book Chapter - Book

  1. Schuler, M. ; Tatibouët, A.
    Strategies towards protection of 1,2- and 1,3-diols in carbohydrate chemistry
    Protecting Groups. Strategies and Applications in Carbohydrate Chemistry. Ed. Wiley-VCH, Weinheim 2019, .

Conference proceedings

  1. Cutolo, G. ; Nehmé, R. ; Lafite, P. ; Fredy, J. W. ; Sabot, C. ; Renard, P. ; Schuler, M. ; Lindhorst, T. K. ; Tatibouët, A.
    Myrosinase-​glucosinolate system: Enzymatic triggered isothiocyanate for bioconjugate chemistry
    Abstracts of Papers, 258th ACS National Meeting & Exposition, San Diego, CA, United States, August 25-29, 2019 2019, CARB-0054.