An efficient and reliable procedure for the preparation of highly reactive rieke zinc

…, L Lutsen, D Vanderzande, W Maes

Index: Kudret, Suleyman; D'Haen, Jan; Lutsen, Laurence; Vanderzande, Dirk; Maes, Wouter Advanced Synthesis and Catalysis, 2013 , vol. 355, # 2-3 p. 569 - 575

Full Text: HTML

Citation Number: 10

Abstract

Abstract Rieke zinc has a wide potential for applications in organic chemistry, notably for the synthesis of highly chemoselective organozinc reagents. However, due to the rather unreliable preparation method, leading to large batch to batch variations, its use has been rather limited. Rieke zinc is commonly prepared by the reduction of zinc chloride with lithium using a stoichiometric amount of naphthalene. In our hands, it was observed that the ...

Related Articles:

Syntheses and Properties of Unsymmetrically Substituted Bi-and Quaterthiophenes.

[Bulletin of the Chemical Society of Japan, , vol. 71, # 2 p. 483 - 495]

Towards a general solid phase approach for the iterative synthesis of conjugated oligomers using a germanium based linker-first solid phase synthesis of an oligo-( …

[Organic and Biomolecular Chemistry, , vol. 5, # 11 p. 1752 - 1763]

Towards a general solid phase approach for the iterative synthesis of conjugated oligomers using a germanium based linker-first solid phase synthesis of an oligo-( …

[Organic and Biomolecular Chemistry, , vol. 5, # 11 p. 1752 - 1763]

Towards a general solid phase approach for the iterative synthesis of conjugated oligomers using a germanium based linker-first solid phase synthesis of an oligo-( …

[Organic and Biomolecular Chemistry, , vol. 5, # 11 p. 1752 - 1763]

Towards a general solid phase approach for the iterative synthesis of conjugated oligomers using a germanium based linker-first solid phase synthesis of an oligo-( …

[Organic and Biomolecular Chemistry, , vol. 5, # 11 p. 1752 - 1763]

More Articles...