CAS: 19891-75-9; 16,16'-Dihydroxylycopene

结构式图片

MSDS等安全信息

    上下游产品

    Dimethyl ψ,ψ-Carotene-16,16'-Dioate 40772-87-0

    合成工艺路线路线简述

    • 合成目标产物 Lycophyll 主要起始原料 ψ,ψ-Carotene-16,16'-Dioic Acid, 16,16'-Dimethyl Ester, (1-Trans,1'-Trans)-
    • (文献来源)合成步骤主要原料 ψ,ψ-Carotene-16,16'-Dioic Acid, 16,16'-Dimethyl Ester, (1-Trans,1'-Trans)-
    📜(2E,6E)-8-Acetoxy-2,6-Dimethylocta-2,6-Dienoic Acid置于四溴化碳,Lithium Methanolate,二异丁基氢化铝,Potassium Carbonate,三苯基膦体系中,用 四氢呋喃,甲醇,水,乙酸乙酯,N,N-二甲基甲酰胺,甲苯 用作溶剂,化学反应 25.0H,反应生成Psi,Psi-胡罗卜素-16,16'-二醇
    参考文献:高效全合成叶绿素(ψ,ψ-胡萝卜素-16,16'-二醇)
    标题:高效全合成叶绿素(ψ,ψ-胡萝卜素-16,16'-二醇)
    摘要:描述了一种使用c10 + C20 + C10合成方法,使用市售材料对叶绿素(16,16'-二羟基-番茄红素;ψ,ψ-胡萝卜素-16,16'-二醇)进行全合成的实用程序香叶醇(c10)和crocetindialdehyde(c20).在八种线性合成步骤中,在大黄素二醛上进行了后期的双重wittig烯化反应,以形成所需的叶绿素支架,同时生成了可以通过HPLC有效分离的多烯几何异构体的混合物.随后,使用c30类胡萝卜素色谱柱通过半制备色谱将全反式糖浆分离至> 95%的纯度.
    Doi:10.1021/op050137F

    海关参考信息

    专利信息


    专利号:US-7247752-B2
    优先权日:2004-10-01
    标 题 :Methods for the synthesis of astaxanthin
    发明人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID
    权利人:CARDAX PHARMACEUTICALS INC
    摘要:A method used for synthesizing intermediates for use in the synthesis of carotenoids and carotenoid analogs, and/or carotenoid derivatives. In some embodiments, the invention includes methods for synthesizing optically active intermediates useful for the synthesis of optically active carotenoids. Synthesis of optically active carotenoids, in one embodiment, may be accomplished by forming an optically active dihydroxy intermediate from ketoisopherone. The optically active dihydroxy intermediate may be converted into optically active astaxanthin derivatives.

    专利号:US-7435861-B2
    优先权日:2005-04-29
    标 题 :Methods for synthesis of carotenoids, including analogs, derivatives, and synthetic and biological intermediates
    发明人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID
    权利人:CARDAX PHARMACEUTICALS INC
    摘要:A method for synthesizing intermediates for use in the synthesis of carotenoid synthetic intermediates, carotenoid analogs, and/or carotenoid derivatives. The carotenoid analog, derivative, or intermediate may be administered to a subject for the inhibition and/or amelioration of any disease that involves production of reactive oxygen species, reactive nitrogen species, radicals and/or non-radicals. In some embodiments, the invention may include methods for synthesizing chemical compounds including an analog or derivative of a carotenoid. Carotenoid analogs or derivatives may include acyclic end groups. In some embodiments, a carotenoid analog or derivative may include at least one substituent. The substituent may enhance the solubility of the carotenoid analog or derivative such that the carotenoid analog or derivative at least partially dissolves in water.

    专利号:US-2008221377-A1
    优先权日:2006-06-16
    标题 :Methods for synthesis of carotenoids, including analogs, derivatives, and synthetic and biological intermediates
    发明人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID; BRAUN CRISTI L
    权利人:LOCKWOOD SAMUEL F; TANG PENG CHO; NADOLSKI GEOFF; JACKSON HENRY L; FANG ZHIQIANG; DU YISHU; YANG MIN; GEISS WILLIAM; WILLIAMS RICHARD; BURDICK DAVID; BRAUN CRISTI L
    摘要:A method for synthesizing intermediates for use in the synthesis of carotenoid synthetic intermediates, carotenoid analogs, and/or carotenoid derivatives. The carotenoid analog, derivative, or intermediate may be administered to a subject for the inhibition and/or amelioration of any disease that involves production of reactive oxygen species, reactive nitrogen species, radicals and/or non-radicals. In some embodiments, the invention may include methods for synthesizing chemical compounds including an analog or derivative of a carotenoid. Carotenoid analogs or derivatives may include acyclic end groups. In some embodiments, a carotenoid analog or derivative may include at least one substituent. The substituent may enhance the solubility of the carotenoid analog or derivative such that the carotenoid analog or derivative at least partially dissolves in water.

    专利号:US-2009099061-A1
    优先权日:2006-01-27
    标 题:Synthesis of carotenoid analogs or derivatives with improved antioxidant characteristics
    发明人:FOSS BENTE J; NADOLSKI GEOFFRY T; LOCKWOOD SAMUEL F
    权利人:FOSS BENTE J; NADOLSKI GEOFFRY T; LOCKWOOD SAMUEL F
    摘要:A method is described for synthesizing and administering carotenoid compounds with improved antioxidant characteristics. In some embodiments, extension or improvement of conjugation may be employed in structural modification of carotenoids. In other embodiments, reduction of ring/chain steric hindrance may improve the lambda max, and hence, the overall antioxidant capability, of particular compounds. In other embodiments, introduction and/or increase in synthetic handles for conjugation may improve the stoichiometric ratios of conjugating moieties to the polyene backbone. The methods may be used to improve natural and/or synthetic compounds for medicinal application in the treatment of disease.

    专利号:US-2006111580-A1
    优先权日:2004-10-01
    标 题 :Methods for the synthesis of chiral dihydroxy ketone intermediates useful for the chiral synthesis of carotenoids

    专利号:US-2006167319-A1
    优先权日:2004-10-01
    标题:Methods for the synthesis of unsaturated ketone intermediates useful for the synthesis of carotenoids

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1126/science.1174621
    摘要:Lingwood D, Simons K. Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 01;327(5961):46–50. doi: 10.1126/science.1174621.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知