CAS: 655246-35-8; (2R,3R,4S,5S,6R)-2-(4-Nitrophenoxy)-6-((Trityloxy)Methyl)Tetrahydro-2H-Pyran-3,4,5-Triol

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35599-02-1 3767-28-0 2492-87-7

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    trityl chloride 4-nitrophenyl-α-D-glucopyranoside 4-nitrophenyl 2,3,4-tri-O-benzoyl-6-O-[2',3',4',6'-tetra-O-benzoyl-5'-deoxy-5'-thio-D-glucopyranosyl]-α-D-glucopyranoside

    合成工艺路线路线简述

    • 合成目标产物 4-Nitrophenyl6-O-Trityl-A-D-Glucopyranoside 主要起始原料 Triphenylmethyl Chloride And 4-Nitrophenyl-Alpha-D-Glucopyranoside
    • (文献来源)合成步骤主要原料 Triphenylmethyl Chloride 和 4-Nitrophenyl-Alpha-D-Glucopyranoside
    📜三苯基氯甲烷,对硝基苯-α-D-葡萄糖吡喃苷置于吡啶体系中,化学反应生成 对硝基苯基 6-O-三苯甲基-Alpha-D-吡喃葡萄糖苷
    参考文献:Synthetic Studies On Oligosaccharides Composed Of 5-Thioglucopyranose Units
    标题:Synthetic Studies On Oligosaccharides Composed Of 5-Thioglucopyranose Units
    摘要:Glycosylation Reactions Of 5-Thioglucopyranosyl Trichloroacetimidates Bearing Ethereal Protective Groups At The 2-O-Position 14-15,And 37 Proceed Smoothly To Give Alpha-Glycosides Stereoselectively By Using A Catalytic Amount Of Silyl Triflate. This Methodology Allowed Us To Achieve Syntheses Of Sulfur-Substituted Isomaltotetraoside 2 And Maltotetraoside 3. These Studies Also Revealed That Benzoyl-Protected 5-Thioglucopyranosyl Trichloroacetimidate 12 Underwent P-Selective Glycosylation With C6-Oh Glucopyranosyl Acceptors Upon Activation By Bf3Oet2. This Was Applied For Preparation Of Sulfur-Substituted Gentiobiosides 1 And 46. (C) 2005 Elsevier Ltd. All Rights Reserved.
    DOI:10.1016/j.Bmc.2005.05.028

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    ✅ COA系统入驻 | 共享模式

    合成参考文献

    参考DOI号:10.1081/CAR-120026464
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