Palladium-catalyzed synthesis of arylamines from diphenyliodonium tetrafluoroborate and secondary amine

Article abstract of DOI:10.1080/00397919608004660

The hetero-cross coupling reaction of diphenyliodonium tetrafluoroborate with secondary amine in the presence of LiNTMS₂ or NaOtBu as base, Pd₂(dba)₃?CHCl₃ as catalyst, and tri-o-tolylphosphine as ligand afforded arylamines at room temperature under mild conditions.

Full text of DOI:10.1080/00397919608004660

This article was downloaded by: [Computing & Library Services, University
of Huddersfield]
On: 28 December 2014, At: 21:55
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
Synthesis of Arylamines
from Diphenyliodonium
Tetrafluoroborate and
Secondary Amine
Suk-Ku Kang a , Hong-Woo Lee a b , Won-Kyu Choi a ,
Ryung-Kee Hong a & Jae-Sun Kim a
a Department of Chemistry , Sung Kyun Kwan
University , Natural Science Campus, Suwon,
440-746, Korea
b Chong Kun Dang Pharm. Co. Ltd.
Published online: 19 Aug 2006.
To cite this article: Suk-Ku Kang , Hong-Woo Lee , Won-Kyu Choi , Ryung-
Kee Hong & Jae-Sun Kim (1996) Palladium-Catalyzed Synthesis of Arylamines
from Diphenyliodonium Tetrafluoroborate and Secondary Amine, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 26:22, 4219-4224, DOI: 10.1080/00397919608004660
To link to this article: http://dx.doi.org/10.1080/00397919608004660
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