Literature DB >> 25497336

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

Erickson M Paragas1, I Abrrey Monreal1, Chris M Vasil1, Jonel P Saludes2.   

Abstract

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 β-elimination reactions in one step to generate the glycal from Neu5Ac1Me. We coined the term One-pot SSA-catalyzed Technology for β-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.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  4-epi-Neu5Ac2en; Acetic anhydride; Microwave synthesis; Neu5Ac2en; Sialic acid; Silica sulfuric acid

Mesh:

Substances:

Year:  2014        PMID: 25497336      PMCID: PMC4281274          DOI: 10.1016/j.carres.2014.09.002

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  17 in total

1.  A facile synthesis of 2-deoxy-2,3-didehydroneuraminic acid derivatives.

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Journal:  Chem Pharm Bull (Tokyo)       Date:  2000-01       Impact factor: 1.645

2.  Chemical insight into the emergence of influenza virus strains that are resistant to Relenza.

Authors:  Fahimeh S Shidmoossavee; Jacqueline N Watson; Andrew J Bennet
Journal:  J Am Chem Soc       Date:  2013-09-03       Impact factor: 15.419

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4.  A facile microwave-assisted protocol for rapid synthesis of N-acetylneuraminic acid congeners.

Authors:  Jonel P Saludes; Dhananjaya Sahoo; I Abrrey Monreal
Journal:  New J Chem       Date:  2014-02-01       Impact factor: 3.591

5.  Preparation of aminoethyl glycosides for glycoconjugation.

Authors:  Robert Sardzík; Gavin T Noble; Martin J Weissenborn; Andrew Martin; Simon J Webb; Sabine L Flitsch
Journal:  Beilstein J Org Chem       Date:  2010-07-29       Impact factor: 2.883

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Authors:  Jonathan Patane; Vincent Trapani; Janice Villavert; Katherine Dawn McReynolds
Journal:  Carbohydr Res       Date:  2009-01-19       Impact factor: 2.104

7.  Synthesis and structural characterization of sialic acid-glutamic acid hybrid foldamers as conformational surrogates of alpha-2,8-linked polysialic acid.

Authors:  Jonel P Saludes; James B Ames; Jacquelyn Gervay-Hague
Journal:  J Am Chem Soc       Date:  2009-04-22       Impact factor: 15.419

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Authors:  Travis Q Gregar; Jacquelyn Gervay-Hague
Journal:  J Org Chem       Date:  2004-02-20       Impact factor: 4.354

9.  Efficient method for the preparation of peracetylated Neu5Ac2en by flash vacuum pyrolysis.

Authors:  Evan J Horn; Jacquelyn Gervay-Hague
Journal:  J Org Chem       Date:  2009-06-05       Impact factor: 4.354

10.  Versatile acetylation of carbohydrate substrates with bench-top sulfonic acids and application to one-pot syntheses of peracetylated thioglycosides.

Authors:  Chin-Sheng Chao; Min-Chun Chen; Shih-Che Lin; Kwok-Kong T Mong
Journal:  Carbohydr Res       Date:  2008-01-26       Impact factor: 2.104

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  2 in total

1.  SialoPen peptides are new cationic foldamers with remarkable cell permeability.

Authors:  I Abrrey Monreal; Erik M Contreras; Gary A Wayman; Hector C Aguilar; Jonel P Saludes
Journal:  Heliyon       Date:  2020-12-24

2.  SnCl4-catalyzed solvent-free acetolysis of 2,7-anhydrosialic acid derivatives.

Authors:  Kesatebrhan Haile Asressu; Cheng-Chung Wang
Journal:  Beilstein J Org Chem       Date:  2019-12-23       Impact factor: 2.883

  2 in total

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