Literature DB >> 15730282

Synthesis, reaction, and recycle of light fluorous Grubbs-Hoveyda catalysts for alkene metathesis.

Masato Matsugi1, Dennis P Curran.   

Abstract

Light fluorous versions of first- and second-generation Grubbs-Hoveyda metathesis catalysts are introduced. These exhibit the expected reactivity profile, are readily recovered from reaction mixtures by fluorous solid-phase extraction, and can be routinely reused five or more times. The catalysts can be used in a stand alone fashion, or supported on fluorous silica gel.

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Year:  2005        PMID: 15730282     DOI: 10.1021/jo048001n

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  7 in total

1.  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

2.  Selective synthesis of (2Z,4E)-dienyl esters by ene-diene cross metathesis.

Authors:  Gustavo Moura-Letts; Dennis P Curran
Journal:  Org Lett       Date:  2007-01-04       Impact factor: 6.005

3.  Plate-to-plate fluorous solid-phase extraction for solution-phase parallel synthesis.

Authors:  Wei Zhang; Yimin Lu; Tadamichi Nagashima
Journal:  J Comb Chem       Date:  2005 Nov-Dec

4.  Automation of fluorous solid-phase extraction for parallel synthesis.

Authors:  Wei Zhang; Yimin Lu
Journal:  J Comb Chem       Date:  2006 Nov-Dec

5.  A fluorous-tagged linker from which small molecules are released by ring-closing metathesis.

Authors:  Stuart G Leach; Christopher J Cordier; Daniel Morton; Gordon J McKiernan; Stuart Warriner; Adam Nelson
Journal:  J Org Chem       Date:  2008-03-08       Impact factor: 4.354

6.  A fluorous-tagged "safety catch" linker for preparing heterocycles by ring-closing metathesis.

Authors:  Catherine O'Leary-Steele; Christopher Cordier; Jerome Hayes; Stuart Warriner; Adam Nelson
Journal:  Org Lett       Date:  2009-02-19       Impact factor: 6.005

7.  Synthesis of natural-product-like molecules with over eighty distinct scaffolds.

Authors:  Daniel Morton; Stuart Leach; Christopher Cordier; Stuart Warriner; Adam Nelson
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

  7 in total

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