Journal of the American Chemical Society

Radical additions of aryl iodides to arenes are facilitated by oxidative rearomatization with dioxygen

DP Curran, AI Keller

Index: Journal of the American Chemical Society, , vol. 128, # 42 p. 13706 - 13707

Full Text: HTML

Citation Number: 107

Abstract

... Miranda, Luis D. Journal of Organic Chemistry (2004), 69 (11), 4001-4004CODEN: JOCEAH ; ISSN:0022-3263. (American Chemical Society). Efficient radical cyclization of alkyl iodides to various arom. systems including pyrrole ...

Related Articles:

Suzuki–Miyaura cross-coupling of aryl and alkyl halides using palladium/imidazolium salt protocols

[Tetrahedron Letters, , vol. 45, # 17 p. 3511 - 3515]

Solvent-Free Microwave-Assisted Suzuki-Miyaura Coupling Catalyzed by PEPPSI-iPr

[Synlett, , # 11 p. 1761 - 1764]

Direct arylation of phenanthroline derivatives via oxidative C–H/C–H cross-coupling: synthesis and discovery of excellent ligands

[Organic and Biomolecular Chemistry, , vol. 11, # 8 p. 1290 - 1293]

Magnetically Separable and Versatile Pd/Fe3O4 Catalyst for Efficient Suzuki Cross??Coupling Reaction and Selective Hydrogenation of Nitroarenes

[Chinese Journal of Chemistry, , vol. 29, # 3 p. 525 - 530]

Convenient synthesis of palladium nanoparticles and catalysis of Hiyama coupling reaction in water

[Organic Letters, , vol. 9, # 18 p. 3639 - 3642]

More Articles...