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多官能团分枝状化合物的合成研究Ⅰ.三方向醚键型分枝状化合物的合成 被引量:3

Synthesis of Multifunctional Groups and Multibranched Compounds Ⅰ. Synthesis of Three directional Ether bond Branched Compounds
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摘要 报道新型有机分子——三方向醚键型分枝状化合物的合成。目标化合物的合成选用甘油为三方向起始核心,以氧丙基为空间间隔基,通过延伸方法解决甘油末端羟基的立体位阻。甘油末端羟基经氰乙基化、醇解、还原和磺酸酯化等步骤制得化合物(4),(4)分别与3种不同的带保护基的分支侧链(1~3)成醚得化合物(5~7),(5~7)脱保护后得羟基数为原母核2倍的醚键型分枝状化合物。所合成的化合物(5~10)均未见文献报道,其结构经IR、1H-NMR和元素分析确证。它们可用于新型多分枝大分子——Cascade分子的合成研究。 New organic molecules the three directional ether bond branched compounds were designed and synthesized. Glycerol used as three directional initiator core was oxypropylated first to decrease steric hindrance. The core(4) reacted respectively with three branched building blocks (1 3) by etherification, followed by deprotection to give title compounds (8 10). The number of the hydroxyl group of the compounds (8 10) are twice as that of initiator core. The structure of all new compounds (5 10) were confirmed by IR, 1H NMR and elemental analysis. These syntheses can be used in the study of new starburst dendritic macromolecules cascade mlecules.
出处 《华西医科大学学报》 CSCD 1996年第4期354-358,共5页 Journal of West China University of Medical Sciences
基金 高等学校博士学科点专项科研基金
关键词 醚键型 分枝状化合物 分支侧链 多官能团 合成 Three directional ether bond branched compounds Initiator core Branched building block Cascade molecules
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  • 1郭丽,翁玲玲,郑虎.六-(ω-羟基丙基)肌醇醚及其衍生物的合成[J].有机化学,1995,15(3):308-311. 被引量:5
  • 2吴勇,翁玲玲,郑虎.多功能桥试剂四(ω-羟丙氧甲基)甲烷及三(ω-羟丙氧甲基)氨甲烷的合成[J].华西医科大学学报,1996,27(2):134-138. 被引量:4
  • 3郭丽,翁玲玲,郑虎.四方向、六方向醚键型分枝状化合物的合成[J].有机化学,1996,16(6):539-543. 被引量:4
  • 4郭丽,有机化学,1996年,16卷,539页
  • 5Newkome G R, Moorefield C N, Vogfle F. Dendritic mac- ro-molecules : concepts, synthesis, perspectives [ J ]. Phys- ics and Chemistry Basis of Biotechnotgy, 1996,9:3-10.
  • 6Padias A B, HKH T R, Tomalis D A, et al. Starburst poly- ether dendrimers [ J ]. J Org Chem, 1987,52:5302-5307.
  • 7Zeny F W,Zirmerman S C. Dendrimers in supramolecular chemistry: from molecular recognition to self-assembly [ J]. Chem Rew, 1997,97 : 1681-1683.
  • 8Chavre S N, Ullapu P R, Min S-J, et aI. Stereocontrolled synthesis of oxaspirobicycles via prints-pinaeol annulation [ J]. Org Lett,2009 ,11:3834-3837.
  • 9Chang Y K, Lo H J, Yan T H. A flexible strategy based on a C2-symmetric poll of chiral substrates : concise synthesis of ( + )-valienamine, key intermediate of ( + )-pancrat- istatin, and conduramines A-1 and E [ J ]. Org Lett,2009,11:4278-4281.
  • 10Tian G Q, Kaiser T, Yang J. Diastereoselective synthesis of syn-I, 3-diols by titanium-mediated reductive coupling of propargylic alcohols [ J]. Org Lett ,2010 ,12 :288-290.

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