Palladium-catalyzed carbonylative cross-coupling of organoboranes with hypervalent iodonium salts: Synthesis of aromatic ketones

Article abstract of DOI:10.1080/00397919808006847

The cross-coupling reaction of organoboronic acids and carbon monoxide (1 atm) with aryl-, alkenyl-, and alkynyliodonium salts at room temperature afforded unsymmetric aromatic ketones in moderate yields.

Full text of DOI:10.1080/00397919808006847

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Palladium-Catalyzed
Carbonylative Cross-Coupling
of Organoboranes with
Hypervalent Iodonium Salts:
Synthesis of Aromatic Ketones
a
a
a
Suk-Ku Kang , Kwon-Ho Lim , Pil-Su Ho , Seok-
a
a
Keun Yoon & Hoe-Joo Son
a
Department of Chemistry , Sung Kyun Kwan
University , Natural Science Campus, Suwon,
440-746, Korea
Published online: 22 Aug 2006.
To cite this article: Suk-Ku Kang , Kwon-Ho Lim , Pil-Su Ho , Seok-Keun Yoon & Hoe-
Joo Son (1998) Palladium-Catalyzed Carbonylative Cross-Coupling of Organoboranes
with Hypervalent Iodonium Salts: Synthesis of Aromatic Ketones, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 28:8, 1481-1489, DOI: 10.1080/00397919808006847
To link to this article: http://dx.doi.org/10.1080/00397919808006847
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