Zobrazeno 1 - 10
of 64
pro vyhledávání: '"J. Bouquant"'
Publikováno v:
Packaging Technology and Science. 16:209-220
Migration of packaging constituents into food may raise concerns about food safety. This paper describes the conclusions of a EU research project (AIR 941025), aiming to facilitate the introduction of migration control into good manufacturing practic
Publikováno v:
Food Additives and Contaminants. 15:100-111
In order to decide whether a plastic food packaging material complies with the European Communities (EC) regulation on migration, a quick analysis of two functional classes of plastics additives (aromatic antioxidants and antistatic agents) from poly
Publikováno v:
Tetrahedron. 52:605-616
The reactivity of 2,2,4,4-tetrasubstituted-1,3-oxazolidines 1 with m-chloroperbenzoic aicd was reinvestigated. Aminoxyls 5 are isolated in good yields in ether at −15 °C, or in anhydrous dichloromethane at 0 °C. Oxaziridines 4 are promoted at roo
Publikováno v:
New Journal of Chemistry. 25:676-678
A convenient and reliable method, based on derivatization and NMR, allows for the assignment of the relative stereochemistry in various substituted cis-1,2-bis(hydroxymethyl)cyclopropanes.
Publikováno v:
ChemInform. 25
Hetero Diels-Alder reaction of oxadienes with 3,4-epoxy-2-methyleneoxolanes gave the corresponding 3,4-epoxy-1,6-dioxaspiro[4,5]-dec-7-enes with high stereoselectivity. Good yields of adducts were obtained in the presence of mild Lewis acis, such as
Publikováno v:
ChemInform. 25
Publikováno v:
ChemInform. 26
Publikováno v:
ChemInform. 26
Publikováno v:
ChemInform. 27
The reactivity of 2,2,4,4-tetrasubstituted-1,3-oxazolidines 1 with m-chloroperbenzoic aicd was reinvestigated. Aminoxyls 5 are isolated in good yields in ether at −15 °C, or in anhydrous dichloromethane at 0 °C. Oxaziridines 4 are promoted at roo
Publikováno v:
Synthesis. 1994:483-485
A new synthesis of α-oxoketene O,N-acetals has been developed from β-oxothioxo esters. Thus, the reaction of 2a-c with alkyl, allyl or cyclic primary amines in refluxing toluene and formic acid led to α-oxoketene O,N-acetals 3a-i in good yields