Suzuki–Miyaura coupling reaction of aryl chlorides using di(2,6-dimethylmorpholino)phenylphosphine as ligand

Suzuki–Miyaura coupling was achieved on a variety of aryl chlorides by using di(2,6-dimethylmorpholino)phenylphosphine (L1) as a bulky electron-rich monoaryl phosphine ligand. We report the couplings of various chlorobenzenes and heteroaryl chlorides. [Display omitted]

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Bibliographic Details
Published in:Tetrahedron 2007-02, Vol.63 (6), p.1345-1352
Main Authors: Cho, Su-Dong, Kim, Ho-Kyun, Yim, Heung-seop, Kim, Mi-Ra, Lee, Jin-Kook, Kim, Jeum-Jong, Yoon, Yong-Jin
Format: Article
Language:English
Subjects:
C–C coupling reaction
Pd-catalyzed coupling of aryl chlorides
PN 2 ligand
Suzuki–Miyaura coupling
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Summary:Suzuki–Miyaura coupling was achieved on a variety of aryl chlorides by using di(2,6-dimethylmorpholino)phenylphosphine (L1) as a bulky electron-rich monoaryl phosphine ligand. We report the couplings of various chlorobenzenes and heteroaryl chlorides. [Display omitted]
ISSN:0040-4020
1464-5416
DOI:10.1016/j.tet.2006.12.001