首页> 外文OA文献 >The first chemical synthesis of novel MeO-3-GlcUA derivative of hyaluronan-based disaccharide to elucidate the catalytic mechanism of hyaluronic acid synthases (HASs)
【2h】

The first chemical synthesis of novel MeO-3-GlcUA derivative of hyaluronan-based disaccharide to elucidate the catalytic mechanism of hyaluronic acid synthases (HASs)

机译:透明质酸基二糖的新型MeO-3-GlcUA衍生物的首次化学合成,阐明了透明质酸合酶(HASs)的催化机理

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The first chemical synthesis of MeO-3-GluUA beta(1 -> 3)GlcNAc-UDP to elucidate the catalytic mechanism of hyalyionic acid synthases (HASS) is described. Construction of the desired beta(1 -> 3)-linked disaccharide 10 was achieved very efficiently by Coupling MeO-3-GlcUA donor 3 with the suitable protected GlCnt(10C) acceptor 4 using BF(3) Et(2)O as Lewis acid Chemoselective removal of anomeric NAP, phosphorylation, hydrogenation, coupling with UMP-morpholidate, and finally complete deprotection gave the target compound 1 in good yield (C) 2009 Elsevier Ltd All rights reserved
机译:描述了MeO-3-GluUA beta(1→3)GlcNAc-UDP的第一化学合成,以阐明透明质酸合酶(HASS)的催化机理。通过使用BF(3)Et(2)O作为Lewis,将MeO-3-GlcUA供体3与合适的受保护GlCnt(10C)受体4偶联,可以非常有效地实现所需的与β(1-> 3)连接的二糖10的构建酸化学选择性除去端基NAP,磷酸化,氢化,与UMP-吗啡酸酯偶联,最后完全脱保护,以高收率得到目标化合物1(C)2009 Elsevier Ltd保留所有权利

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号