Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nicolas Sakkas"'
Autor:
Pauline Poinot, Camélia Kitoun, Matthieu Fonvielle, Quentin Blancart Remaury, Manon Lefresne, Laura Iannazzo, Nicolas Sakkas, Fabiola Djago, Mélanie Etheve-Quelquejeu, Michel Arthur
Publikováno v:
Organic Letters
Organic Letters, 2020, 22 (20), pp.8034-8038. ⟨10.1021/acs.orglett.0c02982⟩
Organic Letters, American Chemical Society, 2020, 22 (20), pp.8034-8038. ⟨10.1021/acs.orglett.0c02982⟩
Organic Letters, 2020, 22 (20), pp.8034-8038. ⟨10.1021/acs.orglett.0c02982⟩
Organic Letters, American Chemical Society, 2020, 22 (20), pp.8034-8038. ⟨10.1021/acs.orglett.0c02982⟩
International audience; Staudinger ligation is an attractive bio-orthogonal reaction that has been widely used to tag proteins, carbohydrates, and nucleic acids. Here, we explore the traceless variant of the Staudinger ligation for 3′-end modificat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f6486e170b4bb14d85ffe178376bd98
https://hal.science/hal-02996863
https://hal.science/hal-02996863
Autor:
Michel Arthur, Tom Brown, Nicolas Sakkas, Ahmed Bouhss, Delphine Patin, Dominique Mengin-Lecreulx, Affaf El Sagheer, Coralie Hoareau, Matthieu Fonvielle, Laura Iannazzo, Mélanie Etheve-Quelquejeu
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2018, 24 (56), pp.14911-14915. ⟨10.1002/chem.201802360⟩
Chemistry-A European Journal, 2018, 24 (56), pp.14911-14915. ⟨10.1002/chem.201802360⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2018, 24 (56), pp.14911-14915. ⟨10.1002/chem.201802360⟩
Chemistry-A European Journal, 2018, 24 (56), pp.14911-14915. ⟨10.1002/chem.201802360⟩
International audience; Conjugation of RNA with multiple partners to obtain mimics of complex biomolecules is limited by the identification of orthogonal reactions. Here, lipid-carbohydrate-peptidyl-RNA conjugates were obtained by post-functionalizat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2a61e985fea19de10ec136369ceae6b
https://hal.sorbonne-universite.fr/hal-01962025
https://hal.sorbonne-universite.fr/hal-01962025
Autor:
Tom Brown, Chloé Le Fournis, Matthieu Fonvielle, Nicolas Sakkas, Laura Iannazzo, Sébastien Cardon, Dominique Mengin-Lecreulx, Emmanuelle Braud, Delphine Patin, Mélanie Etheve-Quelquejeu, Michel Arthur, Afaf H. El-Sagheer
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2016, 55 (43), pp.13553-13557. ⟨10.1002/anie.201606843⟩
Angewandte Chemie (English Edition)
Angewandte Chemie (English Edition), John Wiley & Sons, 2016, 55 (43), pp.13553-13557. 〈10.1002/anie.201606843〉
Angewandte Chemie (English Edition), John Wiley & Sons, 2016, 55 (43), pp.13553-13557. ⟨10.1002/anie.201606843⟩
Angewandte Chemie International Edition, 2016, 55 (43), pp.13553-13557. ⟨10.1002/anie.201606843⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2016, 55 (43), pp.13553-13557. ⟨10.1002/anie.201606843⟩
Angewandte Chemie (English Edition)
Angewandte Chemie (English Edition), John Wiley & Sons, 2016, 55 (43), pp.13553-13557. 〈10.1002/anie.201606843〉
Angewandte Chemie (English Edition), John Wiley & Sons, 2016, 55 (43), pp.13553-13557. ⟨10.1002/anie.201606843⟩
Angewandte Chemie International Edition, 2016, 55 (43), pp.13553-13557. ⟨10.1002/anie.201606843⟩
International audience; RNA functionalization is challenging due to the instability of RNA and the limited range of available enzymatic reactions. We developed a strategy based on solid phase synthesis and post-functionalization to introduce an elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d43bab3d414a2907a7cd5f5547016d6a
https://hal.archives-ouvertes.fr/hal-01440830
https://hal.archives-ouvertes.fr/hal-01440830
Autor:
Mélanie Etheve-Quelquejeu, Emmanuelle Braud, Marco Santarem, Michel Arthur, Jean-Philippe Herbeuval, Nicolas Sakkas, Maryline Chemama, Matthieu Fonvielle, Guillaume Laisné
Publikováno v:
Bioorganicmedicinal chemistry letters. 24(15)
We report here the synthesis of stable Phe-tRNA Phe and Leu-tRNA Leu analogues containing a 1,2,3-triazole ring instead of the ribose-amino acid ester bond. The 1,2,3-triazole ring is generated by dipolar cycloaddition of alkyne Phe and Leu analogues
Autor:
Fonvielle, Matthieu1 matthieu.fonvielle@crc.jussieu.fr, Bouhss, Ahmed2,3, Hoareau, Coralie1, Patin, Delphine2, Mengin‐Lecreulx, Dominique2, Iannazzo, Laura4,5, Sakkas, Nicolas4,5, El Sagheer, Affaf6,7, Brown, Tom7, Ethève‐Quelquejeu, Mélanie4,5 melanie.etheve-quelquejeu@parisdescartes.fr, Arthur, Michel1 michel.arthur@crc.jussieu.fr
Publikováno v:
Chemistry - A European Journal. 10/9/2018, Vol. 24 Issue 56, p14911-14915. 5p.
Autor:
Fonvielle, Matthieu1, Sakkas, Nicolas2,3, Iannazzo, Laura2,3, Le Fournis, Chloé1, Patin, Delphine4, Mengin‐Lecreulx, Dominique4, El‐Sagheer, Afaf5,6, Braud, Emmanuelle2,3, Cardon, Sébastien1, Brown, Tom5, Arthur, Michel1 michel.arthur@crc.jussieu.fr, Etheve‐Quelquejeu, Mélanie2,3 melanie.etheve-quelquejeu@parisdescartes.fr
Publikováno v:
Angewandte Chemie. 10/17/2016, Vol. 128 Issue 43, p13751-13755. 5p.