One-pot SSA-catalyzed β-elimination: an efficient and inexpensive protocol for easy access to the glycal of sialic acid

被引:6
作者
Paragas, Erickson M. [1 ]
Monreal, I. Abrrey [1 ]
Vasil, Chris M. [1 ]
Saludes, Jonel P. [1 ]
机构
[1] Washington State Univ, Dept Chem, Pullman, WA 99164 USA
关键词
Sialic acid; Neu5Ac2en; 4-epi-Neu5Ac2en; Silica sulfuric acid; Microwave synthesis; Acetic anhydride; N-ACETYLNEURAMINIC ACID; MICROWAVE-ASSISTED SYNTHESIS; SULFURIC-ACID; FACILE SYNTHESIS; ACETYLATION; DERIVATIVES; NEURAMINIDASE; ANTAGONISTS; STABILITY; OLIGOMERS;
D O I
10.1016/j.carres.2014.09.002
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
Neu5Ac2en1Me per-OAc, the fully protected glycal of sialic acid, is a key intermediate in the discovery of therapeutics and diagnostics, including anti-influenza drugs and proteolysis resistant peptidomimetic foldamers. The synthesis of this sialic acid derivative, however, still relies on standard sugar chemistry that utilizes multi-step methodologies. Herein we report a facile and highly efficient microwave-assisted preparation of Neu5Ac1Me using silica sulfuric acid (SSA) as solid-supported acid catalyst that is one-to two-orders of magnitude faster than standard procedures. We also describe the microwave-assisted and SSA-catalyzed one-pot, rapid, solvent free reaction that combines both peracetylation and beta-elimination reactions in one step to generate the glycal from Neu5Ac1Me. We coined the term One-pot SSA-catalyzed Technology for beta-Elimination Protocol (OneSTEP) to describe this least laborious, most efficient, and practical preparation to date of Neu5Ac2en1Me per-OAc in terms of yield, time, reagent cost, and waste generation. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:77 / 80
页数:4
相关论文
共 36 条
  • [1] Sialated diazeniumdiolate: A new sialidase-activated nitric oxide donor
    Cai, TB
    Lu, DN
    Landerholm, M
    Wang, PG
    [J]. ORGANIC LETTERS, 2004, 6 (23) : 4203 - 4205
  • [2] Cao HZ, 2012, METHODS MOL BIOL, V808, P31, DOI 10.1007/978-1-61779-373-8_3
  • [3] Synthesis of poly(aspartimide)-based bio-glycoconjugates
    Carlescu, Irina
    Osborn, Helen M. I.
    Desbrieres, Jacques
    Scutaru, Dan
    Popa, Marcel
    [J]. CARBOHYDRATE RESEARCH, 2010, 345 (01) : 33 - 40
  • [4] Versatile acetylation of carbohydrate substrates with bench-top sulfonic acids and application to one-pot syntheses of peracetylated thioglycosides
    Chao, Chin-Sheng
    Chen, Min-Chun
    Lin, Shih-Che
    Mong, Kwok-Kong T.
    [J]. CARBOHYDRATE RESEARCH, 2008, 343 (05) : 957 - 964
  • [5] Microwave-assisted synthesis of N-glycolylneuraminic acid derivatives
    Chopra, Pradeep
    Madge, Paul D.
    Thomson, Robin J.
    Grice, I. Darren
    von Itzstein, Mark
    [J]. TETRAHEDRON LETTERS, 2013, 54 (41) : 5558 - 5561
  • [6] Rapid and clean microwave-assisted synthesis of N-acetylneuraminic acid methyl ester and its β-methyl glycoside
    Chopra, Pradeep
    Thomson, Robin J.
    Grice, I. Darren
    von Itzstein, Mark
    [J]. TETRAHEDRON LETTERS, 2012, 53 (46) : 6254 - 6256
  • [7] Synthesis of oligomers derived from amide-linked neuraminic acid analogues
    Gregar, TQ
    Gervay-Hague, J
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (04) : 1001 - 1009
  • [8] Investigation into an efficient synthesis of 2,3-dehydro-N-acetyl neuraminic acid leads to three decarboxylated sialic acid dimers
    Horn, Evan J.
    Saludes, Jonel P.
    Gervay-Hague, Jacquelyn
    [J]. CARBOHYDRATE RESEARCH, 2008, 343 (05) : 936 - 940
  • [9] Efficient Method for the Preparation of Peracetylated Neu5Ac2en by Flash Vacuum Pyrolysis
    Horn, Evan J.
    Gervay-Hague, Jacquelyn
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2009, 74 (11) : 4357 - 4359
  • [10] Ikeda K, 2000, CHEM PHARM BULL, V48, P163