Literature DB >> 16378490

Ring closing metathesis in the synthesis of biologically interesting peptidomimetics, sugars and alkaloids.

William H C Martin1, Siegfried Blechert.   

Abstract

Olefin metathesis has rapidly established itself as an essential tool in the synthetic chemist's armoury. The ease of operation and functional group tolerance that is obtained with the modern generation of catalysts makes the use of metathesis an extremely attractive option when preparing medicinally interesting molecules. This article will outline some of the ways in which chemists from both industry and academia have been utilising and developing metathesis in the search for novel biological probes and drug leads.

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Year:  2005        PMID: 16378490     DOI: 10.2174/156802605775009757

Source DB:  PubMed          Journal:  Curr Top Med Chem        ISSN: 1568-0266            Impact factor:   3.295


  2 in total

1.  Salicylaldimine Ruthenium Alkylidene Complexes: Metathesis Catalysts Tuned for Protic Solvents.

Authors:  Joseph B Binder; Ilia A Guzei; Ronald T Raines
Journal:  Adv Synth Catal       Date:  2007-02-02       Impact factor: 5.837

2.  Desymmetrization of 7-azabicycloalkenes by tandem olefin metathesis for the preparation of natural product scaffolds.

Authors:  Wolfgang Maison; Marina Büchert; Nina Deppermann
Journal:  Beilstein J Org Chem       Date:  2007-12-18       Impact factor: 2.883

  2 in total

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