Process for producing 3-cephem-4-carboxylic acid derivatives substituted in 3-position
    4.
    发明公开
    Process for producing 3-cephem-4-carboxylic acid derivatives substituted in 3-position 失效
    Verfahren zur Herstellung von 3-Cephem-4Carboxylsäure-Derivaten,substitutioniert in 3。

    公开(公告)号:EP0167651A1

    公开(公告)日:1986-01-15

    申请号:EP84108148.2

    申请日:1984-07-11

    CPC分类号: C12P35/00

    摘要: The subject matter of the invention is a process for producing 3-cephem-4-carboxylic acid derivatives substituted in 3-position of formula (1)

    wherein R 2 is thienyl, diazolyl, thiazolyl, tetrazolyl, thiadiazolyl, thiatriazolyl, oxazolyl, oxadiazolyl, pyridyl, pyrimidinyl, benzothiazolyl, benzimidazolyl, benzoxazolyl or any of their substituted derivatives in any of the possible positions of the mentioned heterocyclic residues available for substitution, which is characterized in that a 7-aminocephalosporanic acid derivative of formula (II)
    wherein R 1 means -OOCCH 2 is reacted with a thiol R 2 SH. The compounds I may be effectively purified by adsorption on a strongly basic anion exchange resin.
    The compounds 1 which are obtained by the process of the invention are valuable intermediates in the synthesis of therapeutically useful cephalosporins.

    摘要翻译: 本发明的主题是制备在式(I)的3-位取代的3-头孢烯-4-羧酸衍生物的方法,其中R 2是噻吩基,二唑基,噻唑基,四唑基,噻二唑基,三唑基,恶唑基, 恶二唑基,吡啶基,嘧啶基,苯并噻唑基,苯并咪唑基,苯并恶唑基或任何可取代的杂环残基的任何可能取代的衍生物,其特征在于式(II)的7-氨基 - 头孢烷酸衍生物 其中R1表示-OOCCH2与硫醇R2SH反应。 化合物I可以通过在强碱性阴离子交换树脂上的吸附而被有效地纯化。 通过本发明的方法获得的化合物I是合成治疗有用的头孢菌素的有价值的中间体。

    METHOD OF OBTAINING NOVEL LUTEIN-BASED FORMULATIONS
    6.
    发明公开
    METHOD OF OBTAINING NOVEL LUTEIN-BASED FORMULATIONS 有权
    VERFAHREN ZUM ERHALTEN NEUER FORMULIERUNGEN AUF LUTEINBASIS

    公开(公告)号:EP1460060A1

    公开(公告)日:2004-09-22

    申请号:EP02796800.7

    申请日:2002-12-20

    IPC分类号: C07C403/02

    CPC分类号: C07C403/24

    摘要: A method of obtaining new formulations based on lutein.
    The present invention describes a method of preparation of formulations of microcrystalline lutein, particularly in the form of esters, which are resistant to oxidation and are soluble in hydrophilic and/or lipophilic media. For these formulations, the esters of lutein are mixed with antioxidants, vegetable oils and/or organic solvents, and this initial mixture is submitted to various stages depending on the type of final formulation required. These formulations are suitable for direct application as colourants in the pharmaceutical, food and cosmetics fields. They can also be used as diet supplements.

    摘要翻译: 获得基于叶黄素的新制剂的方法。 本发明描述了一种制备微晶叶黄素制剂的方法,特别是以酯的形式,它们具有抗氧化作用并且可溶于亲水和/或亲脂性介质。 对于这些制剂,叶黄素的酯与抗氧化剂,植物油和/或有机溶剂混合,并且根据所需的最终制剂的类型将该初始混合物进行各种阶段。 这些制剂适合直接用作制药,食品和化妆品领域的着色剂。 它们也可以用作饮食补充剂。