Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Serge Henrot"'
Publikováno v:
Polymer Engineering and Science
Polymer Engineering and Science, Wiley-Blackwell, 2020, 60 (9), pp.2248-2261. ⟨10.1002/pen.25467⟩
Polymer Engineering and Science, Wiley-Blackwell, 2020, 60 (9), pp.2248-2261. ⟨10.1002/pen.25467⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcc96f7e077cf507995e30c00eca3495
https://hal-cnrs.archives-ouvertes.fr/hal-02941351/document
https://hal-cnrs.archives-ouvertes.fr/hal-02941351/document
Autor:
Noémie Caillol, Maud Rey-Bayle, Alexia Gobrecht, Franck Baco-Antoniali, Jean-Michel Roger, Serge Henrot, Kilani Lamiri, Ryad Bendoula
Publikováno v:
Analytical and Bioanalytical Chemistry
Analytical and Bioanalytical Chemistry, Springer Verlag, 2017, 409 (3), pp.785-796. ⟨10.1007/s00216-016-0064-1⟩
Analytical and Bioanalytical Chemistry, Springer Verlag, 2017, 409 (3), pp.785-796. ⟨10.1007/s00216-016-0064-1⟩
International audience; Controlling production online is an important issuefor chemical companies.Visible and near-infrared (NIR) spectroscopyoffers a number of important advantages for processmonitoring, and has been used since the 1980s. For comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0916db3d8c6ac33e8c47b986de67279f
https://hal.archives-ouvertes.fr/hal-01518418
https://hal.archives-ouvertes.fr/hal-01518418
Autor:
Serge Henrot, M. Larcheveque
Publikováno v:
ChemInform. 21
The preparation of enantiomerically pure β,γ-epoxyesters was achieved by chemoselective opening of β-hydroxybutanolides with trimethylsilyliodide followed by cyclisation of the resulting iodohydrins with silver oxide. The reaction of these epoxyes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b37a2285656d94a5a76fcab84770bcb1
https://doi.org/10.1002/chin.199043123
https://doi.org/10.1002/chin.199043123
Autor:
M. Larcheveque, Serge Henrot
Publikováno v:
Tetrahedron. 43:2303-2310
An efficient stereo- and enantiospecific synthesis of (-) -α-multistriatin from (L)- malic acid is described. The key steps of this synthesis are the stereoselective alkylation of the hydroxylactone 5 and the acid equilibration of the esters 9 and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d93b53e7a71fa0c5d6d82ace6ff3b56a
https://doi.org/10.1016/s0040-4020(01)86814-9
https://doi.org/10.1016/s0040-4020(01)86814-9
Publikováno v:
Synthetic Communications. 16:183-190
Malic acid has been proved to be an extremely valuable chiral synthon for enantiospecific synthesis of complex molecules such as monensin2, amphotericin B3, variou s hydroxytetrahydrofurans4, lactones5,6 and pheromones7. However the (S) isomer only i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfeaee13e41d08267230217a8bcf42a2
https://doi.org/10.1080/00397918608057706
https://doi.org/10.1080/00397918608057706
Publikováno v:
Tetrahedron Letters. 28:5033-5036
The Reduction of 4-O-benzyl-2 -methyl-3-oxo-butyrate esters by several fungal strains produces predominantly (2S,3R)- anti -hydroxyesters in high optical purity. The corresponding (2R,3R)- syn isomer was obtained, with other strains, only in mixture
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::219a19e8bc7b71608c42e7abb39f6be8
https://doi.org/10.1016/s0040-4039(00)96688-7
https://doi.org/10.1016/s0040-4039(00)96688-7
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d88cdd14832bdf2de9252ec734d44ac7
https://doi.org/10.1002/chin.198812364
https://doi.org/10.1002/chin.198812364
Autor:
M. Larcheveque, Serge Henrot
Publikováno v:
ChemInform. 18
An efficient stereo- and enantiospecific synthesis of (-) -α-multistriatin from (L)- malic acid is described. The key steps of this synthesis are the stereoselective alkylation of the hydroxylactone 5 and the acid equilibration of the esters 9 and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea1d54327fa73e5f03d48d2e27c9373c
https://doi.org/10.1002/chin.198740365
https://doi.org/10.1002/chin.198740365
Autor:
Serge Henrot, M. Larcheveque
Publikováno v:
Tetrahedron Letters. 28:1781-1782
The preparation of optically pure β,γ-epoxyesters 3 has been achieved through the opening of 3-hydroxybutanolides with trimethylsilyliodide followed by cyclisation with silver oxyde. They react with organocuprates to afford β-hydroxyesters of high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cdaa8a3024ede38114335dc3b099849
https://doi.org/10.1016/s0040-4039(00)95419-4
https://doi.org/10.1016/s0040-4039(00)95419-4