CAS: 10034-20-5; (2S,3R,4R,5S,6R)-6-(Acetoxymethyl)-3-Aminotetrahydro-2H-Pyran-2,4,5-Triyl Triacetate Hydrochloride

结构式图片

上下游产品

(2S,3R,4R,5S,6R)-6-(acetoxymethyl)-3-((E)-(4-methoxybenzylidene)amino)tetrahydro-2Hpyran-2,4,5-triyl triacetate 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(4-methoxybenzylidene)amino-β-D-glucopyranose 1,3,4,6-tetra-O-acetyl-2-deoxy-2-{[(4-methoxyphenyl)methylidene]amino}-D-glucopyranose -2-deoxy-D-glucopyranose2--2-deoxy-D-glucopyranose 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(3-phenylureido)-β-D-glucopyranose 2-(acetoxymethyl)-5-{[(benzyloxy)carbonyl]amino}tetrahydropyran-3,4,6-triyl triacetate 2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose 1,3,4,6-Tetra-O-acetyl-2-(2,4-dinitroanilino)-2-desoxy-β-D-glucopyranose

合成工艺路线路线简述

    📜1,3,4,6-Tetra-O-Acetyl-2-Deoxy-2-(4-Methoxybenzylidene)Amino-D-α-Glucopyranose置于盐酸体系中,用 丙酮 用作溶剂,以82%的收率获得1,3,4,6-四-O-乙酰基-2-氨基-2-脱氧-β-D-葡萄糖盐酸盐
    参考文献:2-氨基-2-脱氧-D-葡萄糖的n-烷氧羰基衍生物在糖基化反应中作为供体的用途
    标题:2-氨基-2-脱氧-D-葡萄糖的n-烷氧羰基衍生物在糖基化反应中作为供体的用途
    摘要:1,3,4,6-四-O-乙酰基-2-烷氧基羰基氨基-2-脱氧-β-D-Glu复制糖和3,4,6-三-O-乙酰基-2-烷氧基羰基氨基-2-脱氧-α在与模型醇的糖基化反应中,已将-D-吡喃葡萄糖烷基溴用作供体.β-糖苷以高收率和高度的1,2-反式立体选择性获得.恶唑烷酮是一些吡喃葡萄糖基溴化物与低反应性醇反应形成的主要产物,但所有产物的形成都可以通过烷氧基羰基氨基的强烈参与来解释.
    Doi:10.1016/0008-6215(90)84077-8

    海关参考信息

    专利信息


    专利号:US-9550001-B2
    优先权日:2011-06-20
    标 题 :Compositions, methods of synthesis and use of carbohydrate targeted agents
    发明人:TWOROWSKA IZABELA; SIMS-MOURTADA JENNIFER; DELPASSAND EBRAHIM S
    权利人:TWOROWSKA IZABELA; SIMS-MOURTADA JENNIFER; DELPASSAND EBRAHIM S; RADIOMEDIX INC
    摘要:The invention provides D02S derivatives conjugated to monosaccharide ligands directly or through a linker and optionally chelated to a metal, wherein the D02S derivatives having the following structure: wherein R 1 ′, R 2 ′ are each independently —OH or —O-alkyl; R 1 is a hydrogen, a linker, or a ligand; R 3 is a linker and/or a ligand; and n is an integer from 1 to 10; the linker is an amino acid, a peptide, an amino alcohol, a polyethylylene glycol, an alkyl, an alkenyl, an alkynyl, an azide, an aromatic compound, a carboxylic acid, or an ester, the alkyl, alkenyl, or alkynyl is optionally substituted with an alkyl, a halogen, a nitro group, a hydroxyl group, an amino group, or a carboxyl group; the ligand is a GLUT1 targeting moiety.

    专利号:US-2014228551-A1
    优先权日:2011-06-20
    标题 :Compositions, methods of synthesis and use of carbohydrate targeted agents

    专利号:EP-2721045-B1
    优先权日:2011-06-20
    标 题:Compositions, methods of synthesis and use of carbohydrate targeted agents

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    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:A Facile And Efficient Method For Synthesis Of Macrocyclic Lipoglycopeptide
    作者:Qingjie Zhao,Xiang Li,Wenjuan Li,Yan Zou,Honggang Hu,Qiuye Wu |发布日期:2015.2
    摘要:An Efficient And Practical Method For Macrocyclic Lipoglycopeptide Synthesis Was Developed And Utilized To Synthesize Lipoglycosylated Derivatives Of Tyrocidine A. The Method Is Based On Solid-Phase Peptide Synthesis Using 2-Chlorotrityl Resin As The Solid-Phase Support And Lipoglycosyl Amino Acids As Building Blocks. This Synthetic Method Should Be Generally Applicable To Various Macrocyclic Lipoglycopeptides

    合成参考文献


    摘要:U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals., NX#04127
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