Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Julio Mentech"'
Autor:
Isabelle Betremieux, Michel Fontanille, Dhanjay Jhurry, Alain Deffieux, Gérard Descotes, Julio Mentech
Publikováno v:
Die Makromolekulare Chemie. 193:2997-3007
Polymers and copolymers based on the monomethacryloyl ester and the vinylbenzyl ether of sucrose, bearing either blocked or free hydroxyl groups, were synthesized in the presence of free-radical catalysts, and their structures and dimensions were cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::380ab410857895a73900b16d70b795d6
https://doi.org/10.1002/macp.1992.021931206
https://doi.org/10.1002/macp.1992.021931206
Autor:
Veronique Michon, Gérard Descotes, Anne Imberty, Nathalie Roques, Serge Pérez, Julio Mentech, Catherine Hervé du Penhoat
Publikováno v:
Journal of the American Chemical Society. 113:3720-3727
The conformational behavior of aqueous sucrose and its 2-deoxy analogue were studied by NMR and computerized molecular modeling. 'H steady-state NOE and NOESY data are reported along with long-range W-'H coupling constants. In modeling calculations,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff346afdf163bb3d631ee8249cd0f88c
https://doi.org/10.1021/ja00010a014
https://doi.org/10.1021/ja00010a014
Publikováno v:
Carbohydrate Research. 205:323-331
The periodate oxidation of some derivatives of sucrose at primary positions is generally selective for the D-glucopyranoside group. A cleavage at C-2-C3 or C-3-C-4 positions was observed for the 6,1',6'-tri-O-trityl and 6,1',6'-tri-O-(tert-butyldemet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3c7b6607417b4d1facd4af8f5cad99d
https://doi.org/10.1016/0008-6215(90)80150-2
https://doi.org/10.1016/0008-6215(90)80150-2
Publikováno v:
Carbohydrate Research. 188:63-70
A divergent synthesis of 6-deoxy ( 5 ), 4-deoxy ( 9 ), and 3-deoxy ( 15 ) derivatives of sucrose, after acetalation of sucrose with 2,2-dimethoxypropane, is detailed. Thus, 5 was prepared by hydrogenolysis of 6- S -(2-pyridyl)-6-thiosucrose, whereas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31eadd1786c38c54a4a5fa918fe9b613
https://doi.org/10.1016/0008-6215(89)84059-5
https://doi.org/10.1016/0008-6215(89)84059-5
Publikováno v:
Carbohydrate Research. 134:313-320
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c4ca0312e51d564830f9803707e2cd0
https://doi.org/10.1016/0008-6215(84)85047-8
https://doi.org/10.1016/0008-6215(84)85047-8
Sucrochimie IV.1Synthèse régiosétective de dérivés aminés du saccharose via la réaction de Mitsunobu
Publikováno v:
Journal of Carbohydrate Chemistry. 7:21-31
A convenient route for the regiosetective substitution of the primary hydroxyls of sucrose is reported. The application of Mitsunobu's procedure with phthatimide yields. without chromatographic separations, di- cr triphtha-timido derivatives substitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::086e332d6ab1c2fdb888f6e902cbddef
https://doi.org/10.1080/07328308808058901
https://doi.org/10.1080/07328308808058901
Autor:
Julio Mentech, Gérard Descotes
Publikováno v:
Carbohydrate Research. 149:455-457
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80393a6cf893bd4b2b412a496aa21a99
https://doi.org/10.1016/s0008-6215(00)90066-1
https://doi.org/10.1016/s0008-6215(00)90066-1
Publikováno v:
Carbohydrate Research
Carbohydrate Research, 1989, 190 (2), pp.309-312. ⟨10.1016/0008-6215(89)84133-3⟩
Carbohydrate Research, Elsevier, 1989, 190 (2), pp.309-312. ⟨10.1016/0008-6215(89)84133-3⟩
Carbohydrate Research, 1989, 190 (2), pp.309-312. ⟨10.1016/0008-6215(89)84133-3⟩
Carbohydrate Research, Elsevier, 1989, 190 (2), pp.309-312. ⟨10.1016/0008-6215(89)84133-3⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea093761879ea94c885a6bc43696ee2d
https://hal-amu.archives-ouvertes.fr/hal-01744563
https://hal-amu.archives-ouvertes.fr/hal-01744563
