Palladium-catalyzed arylation and vinylation of 2,3-dihydrofuran with hypervalent iodonium salts

Article abstract of DOI:10.1080/00397919708003056

The palladium-catalyzed arylation and vinylation of 2,3-dihydrofuran with aryl and alkenyl iodonium salts afforded 2-phenyl- or 2-alkenyl-2,5-dihydrofurans at room temperatures in an aqueous medium.

Full text of DOI:10.1080/00397919708003056

This article was downloaded by: [Princeton University]
On: 24 September 2013, At: 11:19
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954
Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH,
UK
Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/lsyc20
Palladium-Catalyzed Arylation
and Vinylation of 2,3-
Dihydrofuran with Hypervalent
Iodonium Salts
Suk-Ku Kang a , Tokutaro Yamaguchi a , Jae-Sun Kim a
, Sang-Chul Choi a & Chuljin Ahn a
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 , Tokutaro Yamaguchi , Jae-Sun Kim , Sang-Chul
Choi & Chuljin Ahn (1997) Palladium-Catalyzed Arylation and Vinylation of 2,3-
Dihydrofuran with Hypervalent Iodonium Salts, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 27:6,
1105-1110
To link to this article: http://dx.doi.org/10.1080/00397919708003056
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all the
information (the “Content”) contained in the publications on our platform.
However, Taylor & Francis, our agents, and our licensors make no
representations or warranties whatsoever as to the accuracy, completeness,
or suitability for any purpose of the Content. Any opinions and views

expressed in this publication are the opinions and views of the authors, and
are not the views of or endorsed by Taylor & Francis. The accuracy of the
Content should not be relied upon and should be independently verified with
primary sources of information. Taylor and Francis shall not be liable for any
losses, actions, claims, proceedings, demands, costs, expenses, damages,
and other liabilities whatsoever or howsoever caused arising directly or
indirectly in connection with, in relation to or arising out of the use of the
Content.
This article may be used for research, teaching, and private study purposes.
Any substantial or systematic reproduction, redistribution, reselling, loan,
sub-licensing, systematic supply, or distribution in any form to anyone is
expressly forbidden. Terms & Conditions of access and use can be found at
http://www.tandfonline.com/page/terms-and-conditions