[EN] DELIVERY OF THERAPEUTIC ALKALOID COMPOUNDS [FR] ADMINISTRATION DE COMPOSÉS ALCALOÏDES THÉRAPEUTIQUES
摘要:
Disclosed are compounds that can be converted to mesembrine under physiologically relevant conditions, and related methods of preparing and using the compounds.
Determination of Water Content in Olive Oil by <sup>31</sup>P NMR Spectroscopy
作者:Emmanuel Hatzakis、Photis Dais
DOI:10.1021/jf073227n
日期:2008.3.1
A method for moisture determination in olive oil using 31P NMR spectroscopy is developed. This method is based on the replacement of the hydrogen atoms of water molecules with the tagging agents 2-chloro-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane and diphenylphosphinic chloride. Both reagents were successful in determining moisture in olive oil. However, only the second reagent provided a clean and
PROCESS FOR PRODUCING 1,2-TRANS-GLYCOSIDE COMPOUND
申请人:Otsuka Chemical Co., Ltd.
公开号:EP1849794A1
公开(公告)日:2007-10-31
In preparing a glycoside compound from (a) a furanose compound or pyranose compound, and (b) an alcohol compound, a process for preparing a glycoside compound in which glycosidic bond locates selectively trans form relative to C-2 hydroxyl group, the process comprising using a furanose compound wherein the hydroxyl at the 2-position may have a substituent protected with a group A, or a pyranose compound which may have a substituent
wherein R2 and R3 are the same or different and are each alkyl having 1 to 4 carbon atoms or aryl having or not having a substituent, or R2 and R3 are combined to form alkylene having 2 to 4 carbon atoms (the alkylene may be substituted with alkyl having 1 to 4 carbon atoms, or may have intervening phenylene), and m and n are each an integer of 0 or 1.
在从(a)呋喃糖化合物或吡喃糖化合物和(b)醇化合物制备苷化合物时,制备苷键相对于 C-2 羟基选择性地反式定位的苷化合物的工艺,该工艺包括使用呋喃糖化合物,其中 2 位的羟基可能具有被 A 基团保护的取代基,或使用吡喃糖化合物,其中可能具有取代基
其中R2和R3相同或不同,各自为具有1至4个碳原子的烷基或具有或不具有取代基的芳基,或R2和R3结合形成具有2至4个碳原子的亚烷基(该亚烷基可被具有1至4个碳原子的烷基取代,或可有中间的亚苯基),m和n各自为0或1的整数。
Process for Producing 1,2-Trans-Glycoside Compound
申请人:Yamago Shigeru
公开号:US20080177049A1
公开(公告)日:2008-07-24
In preparing a glycoside compound from (a) a furanose compound or pyranose compound, and (b) an alcohol compound, a process for preparing a glycoside compound in which glycosidic bond locates selectively trans form relative to C-2 hydroxyl group, the process comprising using a furanose compound wherein the hydroxyl at the 2-position may have a substituent protected with a group A, or a pyranose compound which may have a substituent
wherein R
2
and R
3
are the same or different and are each alkyl having 1 to 4 carbon atoms or aryl having or not having a substituent, or R
2
and R
3
are combined to form alkylene having 2 to 4 carbon atoms (the alkylene may be substituted with alkyl having 1 to 4 carbon atoms, or may have intervening phenylene), and m and n are each an integer of 0 or 1.