Literature DB >> 20405840

Efficient bulky phosphines for the selective telomerization of 1,3-butadiene with methanol.

Mathieu J-L Tschan1, Eduardo J García-Suárez, Zoraida Freixa, Hélène Launay, Henk Hagen, Jordi Benet-Buchholz, Piet W N M van Leeuwen.   

Abstract

A series of bulky phosphines containing substituted biphenyl, 2-methylnaphthyl, or 2,7-di-tert-butyl-9,9-dimethylxanthene moiety were prepared. They were used in the preparation of new monophosphine-palladium(0)-dvds complexes, which were employed as catalysts for the selective telomerization of 1,3-butadiene with methanol to obtain 1-methoxyocta-2,7-diene (1-MOD), the key intermediate in the Dow 1-octene process. Several ligands showed improved selectivity and yield compared to that of the benchmark ligand PPh(3). Especially 2,7-di-tert-butyl-9,9-dimethylxanthen-4-yl-diphenylphosphine (4, "mono-xantphos") stands out as an excellent ligand in terms of yield, selectivity, and stability.

Entities:  

Year:  2010        PMID: 20405840     DOI: 10.1021/ja100521m

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


  2 in total

1.  Structure and Reactivity of [(L•Pd)n•(1,5-cyclooctadiene)] (n=1-2) Complexes Bearing Biaryl Phosphine Ligands.

Authors:  Hong Geun Lee; Phillip J Milner; Michael T Colvin; Loren Andreas; Stephen L Buchwald
Journal:  Inorganica Chim Acta       Date:  2014-10-01       Impact factor: 2.545

2.  A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides.

Authors:  Aaron C Sather; Hong Geun Lee; Valentina Y De La Rosa; Yang Yang; Peter Müller; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2015-10-06       Impact factor: 15.419

  2 in total

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