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一步法立体专一性合成游离β-吡喃糖碳苷

Stereospecific Synthesis of Free Hydroxyl β-C-Glycosides in One Sstep
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摘要 Free aldopentoses and aldohexoses reacted respectively with (EtO) 2P(O)CHNaCOAr to give the five stereospecific free hydroxyl \%β\% C glycosides in one step. The reaction take place under a mild condition. The procedures are simple and convenient. The prices of starting materials are cheap. The method can be applied universally for aldopentoses and aldohexoses. The application scope of Wittig Horner reaction has also been expanded. The synthesis of free hydroxyl \%β\% C glycosides from free aldoses directly using Witting\|Horner reaction has not been reported so far. Free aldopentoses and aldohexoses reacted respectively with (EtO) 2P(O)CHNaCOAr to give the five stereospecific free hydroxyl \%β\% C glycosides in one step. The reaction take place under a mild condition. The procedures are simple and convenient. The prices of starting materials are cheap. The method can be applied universally for aldopentoses and aldohexoses. The application scope of Wittig Horner reaction has also been expanded. The synthesis of free hydroxyl \%β\% C glycosides from free aldoses directly using Witting\|Horner reaction has not been reported so far.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2001年第12期2037-2039,共3页 Chemical Journal of Chinese Universities
基金 国家自然科学基金 (批准号 :2 9472 0 34)资助
关键词 合成 WITTIG-HORNER反应 β-吡喃糖碳苷 茂醛糖 已醛糖 C glycosides Synthesis Wittig Horner reaction
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参考文献4

  • 1王文忠,北京医科大学学报,2000年,32卷,277_279页
  • 2王文忠,化学通报,2000年,63卷,11期,42_4页
  • 3李良助,有机合成原理和技术,1992年,94页
  • 4邱东旭,高等学校化学学报,1989年,10卷,5期,158_163页

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