Phosphane‐Free Palladium‐Catalyzed Carbonylative Suzuki Coupling Reaction of Aryl and Heteroaryl Iodides | Zendy

Tambade Pawan J. | Zendy; Patil Yogesh P. | Zendy; Panda Anil G. | Zendy; Bhanage Bhalchandra M. | Zendy

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Phosphane‐Free Palladium‐Catalyzed Carbonylative Suzuki Coupling Reaction of Aryl and Heteroaryl Iodides

Author(s) -

Tambade Pawan J.,

Patil Yogesh P.,

Panda Anil G.,

Bhanage Bhalchandra M.

Publication year - 2009

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200900219

Subject(s) - chemistry , aryl , iodide , catalysis , palladium , carbonylation , coupling reaction , organic chemistry , medicinal chemistry , reaction conditions , combinatorial chemistry , carbon monoxide , alkyl

The carbonylative cross‐coupling reaction of an arylboronic acid with an aryl iodide and a heteroaryl iodide to give unsymmetrical biaryl ketones was carried out by using Pd(tmhd) 2 /Pd(OAc) 2 as a phosphane‐free catalyst. Various aryl and heteroaryl iodides with different arylboronic acid derivatives provided good to excellent yields of the desired products under optimized reaction conditions.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

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