期刊文献+

Tribromoisocyanuric Acid and DABCO-Br as Efficient Catalysts for the Silylation of Hydroxyl Groups with Hexamethyldisilazane 被引量:1

Tribromoisocyanuric Acid and DABCO-Br as Efficient Catalysts for the Silylation of Hydroxyl Groups with Hexamethyldisilazane
下载PDF
导出
摘要 Many primary,secondary,tertiary alcohols,and phenolic hydroxyl groups were effectively converted to their corresponding trimethylsilyl ethers using hexamethyldisilazane in the presence of catalytic amounts of tribromoisocyanuric acid and DABCO-bromine under mild conditions at room temperature with short reaction times in good to excellent yields.Excellent chemoselective silylation of hydroxyl groups in the presence of other functional groups were also observed. Many primary, secondary, tertiary alcohols, and phenolic hydroxyl groups were effectively converted to their corresponding trimethylsilyl ethers using hexamethyldisilazane in the presence of catalytic amounts of tribromoisocyanuric acid and DABCO-bromine under mild conditions at room temperature with short reaction times in good to excellent yields. Excellent chemoselective silylation of hydroxyl groups in the presence of other functional groups were also observed.
出处 《催化学报》 SCIE EI CAS CSCD 北大核心 2008年第9期901-906,共6页
基金 Supported by Bu-Ali Sina University Research Council.
关键词 DABCO-溴 催化剂 催化作用 化学分析 tribromoisocyanuric acid DABCO-bromine hexamethyldisilazane silylation hydroxyl group
  • 相关文献

参考文献40

  • 1Greene T W, Wuts P G M. Protective Groups in Organic Synthesis. 3rd ed. New York: Wiley, 1999. 115-122 被引量:1
  • 2Van Look G, Simchen G, Heberle J. Silylating Agents. 2nd ed. Buches (Switzerland): Fluka, 1995 被引量:1
  • 3Zolfigol M A, Mohammadpoor-Baltork I, Habibi D, Mirjalili B F, Bamoniri A. Tetrahedron Lett, 2003, 44(44):8165 被引量:1
  • 4Corey E J, Snider B B. J Am Chem Soc, 1972, 94(7): 2549 被引量:1
  • 5Olah G A, Gupta B G B, Narang S C, Malhotra R. J Org Chem, 1979, 44(24): 4272 被引量:1
  • 6D'Sa B A, McLeod D, Verkade J G. J Org Chem, 1997, 62(15) : 5057 被引量:1
  • 7Lalonde M, Chan T H. Synthesis, 1985, (9) : 817 被引量:1
  • 8Gautret P, El-ghamarti S, Legrand A, Couturier D, Rigo B. Synth Commun, 1996, 26(4): 707 被引量:1
  • 9Shirini F, Zolfigol M A, Mohammadi K. Phosphorus, Sulfur Silicon Relat Elem , 2003, 178(7) : 1567 被引量:1
  • 10Firouzabadi H, Sardarian A R, Khayat Z, Karimi B, Tangestaninejad S. Synth Commun, 1997, 27 ( 15 ) : 2709 被引量:1

同被引文献27

  • 1Greene T W;Wuts P G.Protective Groups in Organic Synthesis,1999. 被引量:2
  • 2MKucharska et al. 被引量:37
  • 3Mohammad Ali Zolfigol,Gholamabbas Chehardoli,Ezat Ghaemi,Elaheh Madrakian,Reza Zare,Tahereh Azadbakht,Khodabakhsh Niknam,Shadpour Mallakpour.N-Bromo Reagent Mediated Oxidation of Urazoles to Their Corresponding Triazolinediones under Mild and Heterogeneous Conditions[J]Monatshefte für Chemie - Chemical Monthly,2008(3). 被引量:1
  • 4Bose GMondal EKhan A TBordoloi M JTetrahedron Letters. 被引量:1
  • 5IzattR. 被引量:1
  • 6Izatt R. 被引量:1
  • 7Borikar S. 被引量:1
  • 8Kavala VNaik SPatel B KJournal of Organic Chemistry. 被引量:1
  • 9Ali M HStricklin SSynthetic Communications. 被引量:1
  • 10Zolfigol M. 被引量:1

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部