Literature DB >> 15595439

Fluorous tagging strategy for solution-phase synthesis of small molecules, peptides and oligosaccharides.

Wei Zhang1.   

Abstract

The purification of reaction mixtures is a slow process in organic synthesis, especially during the production of large numbers of analogs and compound libraries. Phase-tag methods such as solid-phase synthesis and fluorous synthesis, provide efficient ways of addressing the separation issue. Fluorous synthesis employs functionalized perfluoroalkyl groups attached to substrates or reagents. The separation of the resulting fluorous molecules can be achieved using strong and selective fluorous liquid-liquid extraction, fluorous silica gel-based solid-phase extraction or high-performance liquid chromatography. Fluorous technology is a novel solution-phase method, which has the advantages of fast reaction times in homogeneous environments, being readily adaptable to literature conditions, having easy intermediate analysis, and having flexibility in reaction scale and scope. In principle, any synthetic methods that use a solid-support could be conducted in solution-phase by replacing the polymer linker with a corresponding fluorous tag. This review summarizes the progress of fluorous tags in solution-phase synthesis of small molecules, peptides and oligosaccharides.

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Year:  2004        PMID: 15595439      PMCID: PMC1444942     

Source DB:  PubMed          Journal:  Curr Opin Drug Discov Devel        ISSN: 1367-6733


  22 in total

1.  Oligosaccharide synthesis on a fluorous support.

Authors:  Tsuyoshi Miura; Kohtaro Goto; Daisuke Hosaka; Toshiyuki Inazu
Journal:  Angew Chem Int Ed Engl       Date:  2003-05-09       Impact factor: 15.336

2.  Rapid synthesis of oligosaccharides using an anomeric fluorous silyl protecting group.

Authors:  Leonardo Manzoni
Journal:  Chem Commun (Camb)       Date:  2003-12-07       Impact factor: 6.222

3.  Microwave-assisted synthesis of a 3-aminoimidazo[1,2-a]-pyridine/pyrazine library by fluorous multicomponent reactions and subsequent cross-coupling reactions.

Authors:  Yimin Lu; Wei Zhang
Journal:  QSAR Comb Sci       Date:  2004

4.  "Cap-Tag"-Novel Methods for the Rapid Purification of Oligosaccharides Prepared by Automated Solid-Phase Synthesis Financial support from the donors of the Petroleum Research Fund, administered by the ACS (ACS-PRF 34649-G1), Merck (Predoctoral Fellowship for E.R.P.), Boehringer-Ingelheim (Predoctoral Fellowship for E.R.P.), and the NIH (Biotechnology Training Grant for M.C.H.) is gratefully acknowledged. Funding for the MIT-DCIF Inova 501 was provided by the NSF (Award CHE-9808061). Funding for the MIT-DCIF Avance (DPX) 400 was provided by the NIH (Award 1S10RR13886-01). We thank Silicycle (Quebec City, Canada) for the generous gift of fluorous silica gel and isocyanate silica gel scavenger resin. We thank Dr. O. Plante for helpful discussions and help with the automated oligosaccharide synthesizer.

Authors:  Emma R. Palmacci; Michael C. Hewitt; Peter H. Seeberger
Journal:  Angew Chem Int Ed Engl       Date:  2001-12-03       Impact factor: 15.336

5.  Fluorous Boc ((F)Boc) carbamates: new amine protecting groups for use in fluorous synthesis.

Authors:  Z Luo; J Williams; R W Read; D P Curran
Journal:  J Org Chem       Date:  2001-06-15       Impact factor: 4.354

6.  Solution-phase parallel synthesis of an N-alkylated dihydropteridinone library from fluorous amino acids.

Authors:  Tadamichi Nagashima; Wei Zhang
Journal:  J Comb Chem       Date:  2004 Nov-Dec

7.  Fluorous synthesis of hydantoins and thiohydantoins.

Authors:  Wei Zhang; Yimin Lu
Journal:  Org Lett       Date:  2003-07-10       Impact factor: 6.005

8.  Just add water: a new fluorous capping reagent for facile purification of peptides synthesized on the solid phase.

Authors:  Vittorio Montanari; Krishna Kumar
Journal:  J Am Chem Soc       Date:  2004-08-11       Impact factor: 15.419

9.  Synthesis and reactions of fluorous carbobenzyloxy (FCbz) derivatives of alpha-amino acids.

Authors:  Dennis P Curran; Muriel Amatore; David Guthrie; Matthew Campbell; Eisan Go; Zhiyong Luo
Journal:  J Org Chem       Date:  2003-06-13       Impact factor: 4.354

10.  Fluorous synthesis of disubstituted pyrimidines.

Authors:  Wei Zhang
Journal:  Org Lett       Date:  2003-04-03       Impact factor: 6.005

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  14 in total

1.  Selective metabolite and peptide capture/mass detection using fluorous affinity tags.

Authors:  Eden P Go; Wilasinee Uritboonthai; Junefredo V Apon; Sunia A Trauger; Anders Nordstrom; Grace O'Maille; Scott M Brittain; Eric C Peters; Gary Siuzdak
Journal:  J Proteome Res       Date:  2007-03-08       Impact factor: 4.466

2.  Synthetic applications of fluorous solid-phase extraction (F-SPE).

Authors:  Wei Zhang; Dennis P Curran
Journal:  Tetrahedron       Date:  2006-12-18       Impact factor: 2.457

3.  Fluorous-based small-molecule microarrays for the discovery of histone deacetylase inhibitors.

Authors:  Arturo J Vegas; James E Bradner; Weiping Tang; Olivia M McPherson; Edward F Greenberg; Angela N Koehler; Stuart L Schreiber
Journal:  Angew Chem Int Ed Engl       Date:  2007       Impact factor: 15.336

4.  The azido acid approach to beta-peptides: parallel synthesis of a tri-beta-peptide library by fluorous tagging.

Authors:  Xiao Wang; Scott G Nelson; Dennis P Curran
Journal:  Tetrahedron       Date:  2007-07-02       Impact factor: 2.457

5.  Recent progress on fluorous synthesis of biologically interesting compounds.

Authors:  Zhong-Xing Jiang; Sanjun Zhi; Wei Zhang
Journal:  Mol Divers       Date:  2014-01-20       Impact factor: 2.943

6.  Fluorous mixture synthesis of two libraries with hydantoin-, and benzodiazepinedione-fused heterocyclic scaffolds.

Authors:  Wei Zhang; Yimin Lu; Christine Hiu-Tung Chen; Lu Zeng; Daniel B Kassel
Journal:  J Comb Chem       Date:  2006 Sep-Oct

7.  Fluorous synthesis of sclerotigenin-type benzodiazepine-quinazolinones.

Authors:  Wei Zhang; John P Williams; Yimin Lu; Tadamichi Nagashima; Qainli Chu
Journal:  Tetrahedron Lett       Date:  2007-01-22       Impact factor: 2.415

8.  Fluorous 2,4-Dichloro-1,3,5-triazines (F-DCTs) as Nucleophile Scavengers.

Authors:  Yimin Lu; Wei Zhang
Journal:  QSAR Comb Sci       Date:  2006-07-11

9.  Fluorous 2,4-Dichloro-1,3,5-triazine (F-DCT) as Amide Coupling Agent.

Authors:  Wei Zhang; Yimin Lu
Journal:  QSAR Comb Sci       Date:  2006-07-11

10.  Microwave-Enhanced High-Speed Fluorous Synthesis.

Authors:  Wei Zhang
Journal:  Top Curr Chem       Date:  2006-08-30
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