Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Pierre Angibeaud"'
Autor:
Carole Migné, Elisabeth Grenet, Pierre Angibeaud, Gérard Prensier, Agnès Cornu, Jean-Pierre Utille
Publikováno v:
Journal of the Science of Food and Agriculture. 78:373-381
Two phenolic compounds, p-coumaric acid and feruloyl-arabinose, were localised by immunocytochemistry in the cell walls of the apical internode of two lines of maize (Co125 and W401) of different digestibility. The compounds were detected at two stag
Autor:
Pierre Angibeaud, Jean-Pierre Utille
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 24
Poly(glucose-pyrrole) modified electrodes: A novel chiral electrode for enantioselective recognition
Autor:
Jean-Claude Moutet, François Tran-Van, Pierre Angibeaud, Eric Saintl-Aman, Jean-Pierre Utille
Publikováno v:
Advanced Materials. 4:511-513
Autor:
Carole Migné, Agnès Cornu, Elisabeth Grenet, Jean-Pierre Utille, G. Prensier, Pierre Angibeaud
Publikováno v:
Journal of the Science of Food and Agriculture
Journal of the Science of Food and Agriculture, Wiley, 1999, 79 (9), pp.1163-1170. ⟨10.1002/(SICI)1097-0010(19990701)79:93.3.CO;2-W⟩
Journal of the Science of Food and Agriculture, Wiley, 1999, 79 (9), pp.1163-1170. ⟨10.1002/(SICI)1097-0010(19990701)79:93.3.CO;2-W⟩
International audience; Immunogold labelling of feruloyl-arabinose was performed on the base and the top of the apical internode of the stem of Co125 and W401 maize, harvested at anthesis +5 days, after incubation in the rumen in nylon bags for 4, 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06ff3872a3b73853dc9ffa1f4d322a9e
https://hal.archives-ouvertes.fr/hal-00309777
https://hal.archives-ouvertes.fr/hal-00309777
Autor:
Pierre Angibeaud, Jean-Pierre Utille
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1490-1492
Treatment of methyl β-D-glycopyranosides with TMSOtf–Ac2O gives acyclic products by selective cleavage of the ring carbon–oxygen bond, whereas methyl α-D-isomers undergo replacement of the anomeric methoxy by an acetoxy group with retention of
Publikováno v:
Carbohydrate Research
Carbohydrate Research, Elsevier, 1990, pp.403-407
Carbohydrate Research, Elsevier, 1990, pp.403-407
On obtient un compose O-[acetoxy-«1» penta-O acetyl-2,3,4,5,6 glucityl]-6 tetra-O-acetyl-1,2,3,4 glucopyranose qui reagit ensuite avec le methanolate de sodium et donne le D-glucose penta-O-acetyle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c529aa59970ad02452de0a9bcb390037
https://hal.archives-ouvertes.fr/hal-00310212
https://hal.archives-ouvertes.fr/hal-00310212
Autor:
Jean-Pierre Utille, Pierre Angibeaud
Publikováno v:
Synthesis. 1991:737-738
Regioselective acetolysis of cyclomaltohexaose perbenzyl ethers at C-6 with acetic anhydride in the presence of trimethylsilyl trifluoromethanesulfonate at low temperature constitutes an easy route to the C-6 acetylated intermediate 2. Further transf
Autor:
Pierre Angibeaud, Claudine Cohen-Addad, Michel Thomas, Jacques Defaye, Claude Bosso, Derek Horton
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1583-1592
Deamination of 2-amino-2-deoxy-D-glucose ethylene dithioacetal (1) at pH 5.6, followed by acetylation of the product, gave an 8 : 40 : 3 mixture of 3,5,6-tri-O-acetyl-1,2-SS′-ethylene-1,2-dithio-α-D-mannofuranoside (5b), 3,4,6-tri-O-acetyl-1,2-SS
Publikováno v:
Carbohydrate Research. 78:195-204