Xiao-Feng Wu

 

Xiao-Feng Wu

Leibniz-Institut für Katalyse an der Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock, Germany
E-mail: xiao-feng.wu@catalysis.de

- See more at: http://organicchemistrysite.blogspot.in/2015/09/pdc-as-efficient-heterogeneous-catalyst.html#sthash.DJ9opGcC.dpuf

Leibniz-Institut für Katalyse e.V. an der Universitüt Rostock Albert-Einstein-Strasse 29a, 18059 Rostock, Germany
 E-mail: xiao-feng.wu@catalysis.de
Tel: +49-381-1281-343

Leibniz-Institut für Katalyse an der Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock, Germany
E-mail: xiao-feng.wu@catalysis.de

- See more at: http://organicchemistrysite.blogspot.in/2015/09/pdc-as-efficient-heterogeneous-catalyst.html#sthash.DJ9opGcC.dpuf

Xiao-Feng Wu was born in 1985 in China. He studied chemistry in Zhejiang Sci-Tech University (ZSTU), where he obtained his BSc degree in science in 2007. In the same year, he moved to Rennes 1 University in France and worked with Prof C. Darcel on iron-catalyzed reactions. After earning his Master’s degree in 2009, he joined Matthias Beller’s group in the Leibniz Institute for Catalysis (LIKAT) in Germany, where he completed his PhD thesis in January 2012. He subsequently began independent research at ZSTU and LIKAT. His research interests include carbonylation reactions, synthesis of heterocycles and the catalytic application of cheap metals. He was also a Fellow of the Max-Buchner-Forschungsstiftung.

Phone:	343
	Cell Phone:
	Fax:	+49(381)1281-51343
	Department:	Beller, Prof. Matthias
	Street:	A.-Einstein-Str. 29a
	City:	Rostock
	ZIP Code:	18059
	Email:	Xiao-Feng.Wu@catalysis.de
	Room:	2.021
	Full Name:	Herr Dr. Xiao-Feng Wu

Leibniz-Institut für Katalyse an der Universität Rostock, Albert-Einstein-Straße 29a, 18059 Rostock, Germany
E-mail: xiao-feng.wu@catalysis.de

- See more at: http://organicchemistrysite.blogspot.in/2015/09/pdc-as-efficient-heterogeneous-catalyst.html#sthash.DJ9opGcC.dpuf

The 4(3H)-quinazolinone is a frequently encountered heterocycle with broad applications including antimalarial, antitumor, anticonvulsant, fungicidal, antimicrobial, and anti-inflammatory. The current review article will briefly outline the new routes and strategies for the synthesis of valuable 4(3H)-quinazolinones.

Recent advances in 4(3H)-quinazolinone syntheses

Lin He,^a   Haoquan Li,^a   Jianbin Chen^a and   Xiao-Feng Wu*^a  

*Corresponding authors

^aLeibniz-Institut für Katalyse e.V., Albert Einstein Straße. 29a, 18059 Rostock, Germany
E-mail: xiao-feng.wu@catalysis.de
Tel: +49-381-1281-343

 

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