CAS: 68856-96-2; Boc-D-Tyr(Me)-Oh

该化合物是一个受保护的氨酸衍生物,通常用于丙酸合成和有机化学."乙酸"(乙基-丁基氧碳基)组是氨基功能的保护组,允许有选择的反应,而不会干扰该矿."D-Tyr"表示氨基酸是硫酸D-抗氧素的,在各种生物化学应用中非常重要."Me"表示一种与乙基氢盐酸苯丙基相连的甲基组,可加强其脂性与稳定性.该化合物一般是白色到非白固态的,在有机溶剂(如乙醇和二甲基硫氧化物(DMSO)中可溶解,但水中可溶性较小.在标准实验室条件下,其稳定性使其适合各种合成应用,特别是在形成peptid 联系中."Me"组的存在使得在酸性条件下易于脱氧基质的甲基混合物,有助于在酸性条件下全面进行化学合成.

结构式图片

相似化合物

141895-35-4 53267-93-9 6230-11-1

上下游产品

CAS号94790-24-6 (S)-2-((叔丁氧羰基)氨... | CAS号24424-99-5 二碳酸二叔丁酯 | CAS号556-02-5 D-酪氨酸 | CAS号76757-90-9 丁氧羰基-D-酪氨酸-甲氧基酯 | CAS号3728-20-9 D-酪氨酸甲酯盐酸盐 | CAS号830-09-1 4-甲氧基肉桂酸 | CAS号832-01-9 3-(4-甲氧基苯基)-2-丙酸甲酯 | CAS号241153-85-5 methyl 3-(3-chl...

合成工艺路线路线简述

    4-甲氧基肉桂酸置于ad-Mix Beta,氯化亚砜,甲基磺酰胺,H6O6Os(2-)*2K(1+),叠氮磷酸二苯酯,Palladium On Activated Charcoal,水,氢气,Potassium Carbonate,1,8-二氮杂双环[5.4.0]十一碳-7-烯,Potassium Hexacyanoferrate(Iii)体系中,用 四氢呋喃,甲醇,水,乙酸乙酯,叔丁醇 作为反应溶剂,化学反应 77.0H,反应生成 N-Boc-4-甲氧基-D-苯基丙氨酸
    参考文献:通过sharpless不对称二羟基化合成隐霉素24单元b
    标题:通过sharpless不对称二羟基化合成隐霉素24单元b
    摘要:已经使用sharpless不对称二羟基化作为关键步骤,开发了一种用于合成隐藻素24单元b的合成途径.这项研究表明,使用二苯基磷酰基叠氮化物直接叠氮化α-羟基酸酯有利于α-氨基酸的不对称合成,而在转化过程中不会失去手性.
    DOI:10.1016/j.Tetlet.2012.10.078

    海关参考信息

    专利信息


    专利号:US-2004110228-A1
    优先权日:2002-04-01
    标 题:Combinatorial organic synthesis of unique biologically active compounds
    发明人:MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
    摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

    专利号:WO-9834113-A1
    优先权日:1997-02-04
    标题 :Combinatorial libraries of bicyclic guanidine derivatives and compounds therein
    发明人:OSTRESH JOHN M; MEYER JEAN-PHILIPPE; DOOLEY COLETTE T; HOUGHTEN RICHARD A; BLONDELLE SYLVIE E; SCHONER CHRISTA C
    权利人:TREGA BIOSCIENCES INC
    摘要:The invention provides a rapid approach for combinatorial synthesis and screening of combinatorial libraries of bicyclic guanidine compounds. The present invention further provides the compounds made by the combinatorial synthesis and individually as well as methods of using the same.

    专利号:US-6359144-B1
    优先权日:1997-02-04
    标 题 :Combinatorial libraries of bicyclic guanidine derivatives and compounds therein
    发明人:OSTRESH JOHN M; MEYER JEAN-PHILIPPE; DOOLEY COLETTE T; BLONDELLE SYLVIE E; SCHONER CHRISTA C; HOUGHTEN RICHARD A
    权利人:LION BIOSCIENCE AG
    摘要:The invention provides a rapid approach for combinatorial synthesis and screening of combinatorial libraries of bicyclic guanidine compounds. The present invention further provides the compounds made by the combinatorial synthesis and individually as well as methods of using the same.
    四川嘉瑛莱科技有限责任公司
    ⚠️ 未注册 · 未认证企业
    ⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
    数据来源于公开网络搜索,平台未作核实,请自行辨别。
    🏢敬请 企业认领
    🏬开设公司展台
    📢获取免费会员权益
    🎖️点亮专属注册企业标签
    📇展现公司完整信息 样本查看立即注册认领 →
    网址: http://www.jiayinglai.com/
    电话: 028-64159575👤
    📞四川嘉瑛莱科技有限责任公司 ⚠️参考联系方式

    销售电话:028-64159575
    邮箱:linda@enlaibio.com
    🆔 联系时候可告知是从"百琢研"平台获取的信息.
    ⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

    ⚠️ 未注册 · 未认证企业
    注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别 ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
    第 1 / 1 页
    现货

    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

    主要参考文献

    参考标题:Total Synthesis Of Cryptophycins. Revision Of The Structures Of Cryptophycins A And C
    作者:Russell A. Barrow,Thomas Hemscheidt,Jian Liang,Seunguk Paik,Richard E. Moore,Marcus A. Tius |发布日期:1995.3
    摘要:The Convergent Total Synthesis Of Cryptophycins C And D Is Described. It Has Been Shown That In Both Natural Products The Absolute Configuration Of The A-Amino Acid Corresponds To The D-Series. The Structural Assignment For Cryptophycin C Has Been Corrected To Reflect This Fact. Since The Structure Of Cryptophycin A Has Been Correlated To Cryptophycin C, The Chloro-0-Methyltyrosine Unit In Cryptophycin

    合成参考文献


    参考文献:10.1055/s-2006-950332
    摘要:Sewald N, Eißler S, Stoncius A, Nahrwold M. The Synthesis of Cryptophycins. Synthesis. 2006 Nov;2006(22):3747–89. doi: 10.1055/s-2006-950332.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知