Convenient one-pot synthesis of aldehydes from carboxylic acid chlorides with sodium diethyldihydroaluminate

Article abstract of DOI:10.1080/00397919308011276

Carboxylic acid chlorides and acids were converted into the corresponding aldehydes conveniently in one-pot process with sodium diethyldihydroaluminate (SDDA) in moderate to good yields.

Full text of DOI:10.1080/00397919308011276

This article was downloaded by: [Columbia University]
On: 08 December 2014, At: 03:33
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
Convenient One-Pot Synthesis
of Aldehydes from Carboxylic
Acid Chlorides with Sodium
Diethyldihydroaluminate
Nung Min Yoon a , Kyung Il Choi a , Young Soo Gyoung
a & Wan Sik Jun b
a Department of Chemistry , Sogang University ,
Seoul, 121-742, Korea
b Department of Chemistry , Kangreung National
University , Kangreung, 210-702, Korea
Published online: 23 Sep 2006.
To cite this article: Nung Min Yoon , Kyung Il Choi , Young Soo Gyoung & Wan Sik Jun
(1993) Convenient One-Pot Synthesis of Aldehydes from Carboxylic Acid Chlorides
with Sodium Diethyldihydroaluminate, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 23:12, 1775-1781,
DOI: 10.1080/00397919308011276
To link to this article: http://dx.doi.org/10.1080/00397919308011276
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