Literature DB >> 16866499

Highly active molybdenum-alkylidyne catalysts for alkyne metathesis: synthesis from the nitrides by metathesis with alkynes.

Robyn L Gdula1, Marc J A Johnson.   

Abstract

Terminal nitrido complexes NMo(OC(CF3)2Me)3 (4), NMo(OC(CF3)2Me)3(NCMe) (4-NCMe), and NMo(OC(CF3)3)3(NCMe) (5-NCMe) react irreversibly with 3-hexyne at elevated temperature in hydrocarbon solution to form the corresponding propylidyne complexes EtCMo(OC(CF3)2Me)3 (3) and EtCMo(OC(CF3)3)3 (6), long known as exceptionally active catalysts for alkyne metathesis. The propylidyne complexes are isolated as the more readily crystallized 1,2-dimethoxyethane (DME) adducts for convenience; 3-DME is isolated in 61% yield on a multigram scale.

Entities:  

Year:  2006        PMID: 16866499     DOI: 10.1021/ja058036k

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  3 in total

1.  Recent advances in the development of alkyne metathesis catalysts.

Authors:  Xian Wu; Matthias Tamm
Journal:  Beilstein J Org Chem       Date:  2011-01-18       Impact factor: 2.883

2.  The Ascent of Alkyne Metathesis to Strategy-Level Status.

Authors:  Alois Fürstner
Journal:  J Am Chem Soc       Date:  2021-09-14       Impact factor: 15.419

3.  Terminal uranium(V)-nitride hydrogenations involving direct addition or Frustrated Lewis Pair mechanisms.

Authors:  Lucile Chatelain; Elisa Louyriac; Iskander Douair; Erli Lu; Floriana Tuna; Ashley J Wooles; Benedict M Gardner; Laurent Maron; Stephen T Liddle
Journal:  Nat Commun       Date:  2020-01-17       Impact factor: 14.919

  3 in total

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