A highly efficient deprotection of the 2,2,2-trichloroethyl group at the anomeric oxygen of carbohydrates

被引:6
|
作者
Zhang, Jianbo [1 ]
Fu, Jie [1 ]
Si, Wenshuai [1 ]
Wang, Xiaohu [1 ]
Wang, Zhongfu [2 ]
Tang, Jie [1 ]
机构
[1] E China Normal Univ, Dept Chem, Shanghai 200062, Peoples R China
[2] NW Univ Xian, Sch Life Sci, Xian 710069, Peoples R China
基金
上海市自然科学基金;
关键词
2,2,2-Trichloroethyl; Anomeric center; Carbohydrates; Deprotection; Zinc dust; STEREOSELECTIVE TOTAL-SYNTHESIS; GLYCOSYL HEMIACETALS; HYDROLYSIS; OLIGOSACCHARIDES; THIOGLYCOSIDES; DEACYLATION; MILD;
D O I
10.1016/j.carres.2011.08.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Commercially available zinc dust in the presence of ammonium chloride in acetonitrile at reflux removes the 2,2,2-trichloroethyl (ICE) group at anomeric centers with excellent yields (>95%) in short reaction times. This present method is easily implemented on substrates containing acyl and benzyl groups and large-scale reactions also proceed in high yield. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2290 / 2293
页数:4
相关论文
共 50 条
  • [31] N-alkylation of N-(2,2,2-trichloroethyl)arenesulfonamides
    I. B. Rozentsveig
    A. V. Popov
    G. G. Levkovskaya
    Russian Journal of Organic Chemistry, 2013, 49 : 466 - 468
  • [32] N-alkylation of N-(2,2,2-trichloroethyl)arenesulfonamides
    Rozentsveig, I. B.
    Popov, A. V.
    Levkovskaya, G. G.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2013, 49 (03) : 466 - 468
  • [33] Preparation of Substituted Benzimidazoles and Imidazopyridines Using 2,2,2-Trichloroethyl Imidates
    Caron, Stephane
    Jones, Brian P.
    Wei, Lulin
    SYNTHESIS-STUTTGART, 2012, 44 (19): : 3049 - 3054
  • [34] Reaction of N-(2,2,2-trichloroethyl)arenesulfonamides with activated alkenes
    Rozentsveig, IB
    Evstaf'eva, IT
    Levkovskaya, GG
    Mirskova, AN
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2005, 41 (10) : 1561 - 1563
  • [35] New developments towards the synthesis and utilization of 2,2,2-trichloroethyl aryldiazoacetates
    Mighion, Jeffrey
    Fu, Liangbing
    Davies, Huw
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2016, 252
  • [36] 2,2,2-TRICHLOROETHYL CHLOROFORMATE - GENERAL REAGENT FOR DEMETHYLATION OF TERTIARY METHYLAMINES
    MONTZKA, TA
    MATISKEL.JD
    PARTYKA, RA
    TETRAHEDRON LETTERS, 1974, (14) : 1325 - 1327
  • [37] 4′-Chlorobiphenyl-3-yl 2,2,2-trichloroethyl sulfate
    Li, Xueshu
    Parkin, Sean
    Duffel, Michael W.
    Robertson, Larry W.
    Lehmler, Hans-Joachim
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2010, 66 : O2306 - U305
  • [38] DEPRESSANT AND ANTI-CONVULSANT PROPERTIES OF SOME 2,2,2-TRICHLOROETHYL ESTERS
    AGGARAWAL, RK
    DHARIWAL, MA
    HUTCHINS, DA
    SUGDEN, JK
    PHARMACEUTICA ACTA HELVETIAE, 1983, 58 (04): : 112 - 114
  • [40] HYDROLYSIS OF DIMETHYL (L-ACETOXY-2,2,2-TRICHLOROETHYL)-PHOSPHONATE
    ANDREEVA, LS
    ANDRIANO.AA
    BELSKII, VE
    VAVILOVA, MF
    GURYLEV, EA
    NIKONORO.KV
    IZVESTIYA AKADEMII NAUK SSSR-SERIYA KHIMICHESKAYA, 1971, (10): : 2336 - &