Zirconocene catalysis in the synthesis of 1,4-dimagnesium reagents: using competitive inhibition to suppress β-hydrogen abstraction

Substituted 1,4-dimagnesium reagents were synthesized by the zirconocene-catalyzed reaction of alkenes with ethylmagnesium reagents in the presence of a methylmagnesium containing additive. Improved selectivity for formation of dimagnesium reagents over monomagnesium reagents was obtained in the pre...

Full description

Saved in:
Bibliographic Details
Published in:Transition metal chemistry (Weinheim) 2010-09, Vol.35 (6), p.695-698
Main Authors: Fielding, Elisha N., Gao, Yan S., Knight, Kyle S.
Format: Article
Language:English
Subjects:
Catalysis
Chemistry
Chemistry and Materials Science
Inorganic Chemistry
Organometallic Chemistry
Physical Chemistry
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Substituted 1,4-dimagnesium reagents were synthesized by the zirconocene-catalyzed reaction of alkenes with ethylmagnesium reagents in the presence of a methylmagnesium containing additive. Improved selectivity for formation of dimagnesium reagents over monomagnesium reagents was obtained in the presence of the methylmagnesium containing additive. The ratio of mono- to dimagnesiated products was extrapolated from the ratio of alkene to diene in the products formed when the reaction was quenched with allyl bromide. The extent of the increase in the alkene/diene ratio was dependent on the type of organomagnesium halide, with greatest increases (59%) for the alkylmagnesium chlorides. A mechanism for improved selectivity by suppression of β-hydrogen abstraction in the catalytic cycle is presented. Quenching the 1,4-dimagnesium reagents with allyl bromide yielded decadienes.
ISSN:0340-4285
1572-901X
DOI:10.1007/s11243-010-9381-y