Facile palladium-catalyzed synthesis of 3-oxo-1,3-dihydro-1- isobenzofuranyl alkanoates from 2-bromobenzaldehyde and carboxylic acids

Article abstract of DOI:10.1080/00397910008087130

2-Bromobenzaldehyde reacts with carboxylic acids in acetonitrile under carbon monoxide pressure in the presence of a catalytic amount of a palladium catalyst to give the corresponding 3-oxo-1,3-dihydro-1-isobenzofuranyl alkanoates in high yields.

Full text of DOI:10.1080/00397910008087130

This article was downloaded by: [Stony Brook University]
On: 21 October 2014, At: 18:42
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
Facile Palladium-Catalyzed
Synthesis of 3-oxo- 1,3-
Dihydro-1-Isobenzofuranyl
Alkanoates From 2-
Bromobenzaldehyde and
Carboxylic Acids
a
a
a
Chan Sik Cho , Dong Yeol Baek , Hye-Young Kim
,
a
b
Sang Chul Shim & Dae Hee Oh
a
Department of Industrial Chemistry , College of
Engineering, Kyungpook National University , Taegu,
7
02-701, Korea
b
Department of Surface Coating Engineering ,
Pukyung National University , Pusan, 608-739, Korea
Published online: 04 Dec 2007.
To cite this article: Chan Sik Cho , Dong Yeol Baek , Hye-Young Kim , Sang Chul Shim
&
Dae Hee Oh (2000) Facile Palladium-Catalyzed Synthesis of 3-oxo- 1,3-Dihydro-1-
Isobenzofuranyl Alkanoates From 2-Bromobenzaldehyde and Carboxylic Acids,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 30:6, 1139-1145, DOI: 10.1080/00397910008087130
To link to this article: http://dx.doi.org/10.1080/00397910008087130
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