Abstract The reaction of N,N-diethylamino-tributyltin with aryl bromides in the presence of a catalytic amount of PdCl2(o-tolyl3P)2 gave N,N-diethylaminobenzene derivatives. The reaction is a new kind of amination different from ones through aryne or SRN1 mechanise

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Kosugi et al. (Wed,) studied this question.

synapsesocial.com/papers/69fc75f19a4328ddd8fa409d https://doi.org/https://doi.org/10.1246/cl.1983.927

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Palladium-catalyzed Exchange of Allylic Groups of Ethers and Esters with Active Hydrogen Compounds. II.1972 · 115 citations
2Palladium-catalyzed amidation of aryl, heterocyclic, and vinylic halides1974 · 671 citations
3Aromatic substitution by the SRN1 mechanism1978 · 603 citations
4Palladium-catalyzed Exchange of Allylic Groups of Ethers and Esters with Carboxylic Anhydrides1973 · 13 citations
5The Rearrangement of Phenyl Allyl Ethers<sup>1</sup>1936 · 29 citations

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Palladium-catalyzed Exchange of Allylic Groups of Ethers and Esters with Active Hydrogen Compounds. II.1972 · 115 citations
2Palladium-catalyzed amidation of aryl, heterocyclic, and vinylic halides1974 · 671 citations
3Aromatic substitution by the SRN1 mechanism1978 · 603 citations
4Palladium-catalyzed Exchange of Allylic Groups of Ethers and Esters with Carboxylic Anhydrides1973 · 13 citations
5The Rearrangement of Phenyl Allyl Ethers<sup>1</sup>1936 · 29 citations