Keiji
Maruoka
a,
Benjamin
List
b,
Hisashi
Yamamoto
c and
Liu-Zhu
Gong
d
aDepartment of Chemistry, Graduate School of Science, Kyoto University, Kyoto, 606-8502, Japan. E-mail: maruoka@kuchem.kyoto-u.ac.jp; Tel: +81-75-753-4041
bMax-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, D-45470 Mülheim an der Ruhr, Germany. E-mail: list@mpi-muelheim.mpg.de; Tel: +49-208-306-2411
cDepartment of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, IL 60637. E-mail: yamamoto@uchicago.edu; Tel: 773-702-5059
dHefei National Laboratory for Physical Sciences at the Microscale, Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China. E-mail: gonglz@ustc.edu.cn; Tel: +86-(0)551-3600671
Keiji Maruoka | Keiji Maruoka is currently Professor of Chemistry at the Graduate School of Science, Kyoto University. His research focuses on bidentate Lewis acid chemistry, asymmetric phase-transfer catalysis, and the design and synthetic utility of high-performance organocatalysts. |
Benjamin List | Prof. Dr. Benjamin List, is the managing director of the Max-Planck-Institut für Kohlenforschung in Mülheim an der Ruhr, Germany and a honorary professor of chemistry at the University of Cologne. His research focuses on developing new catalysis concepts. |
Hisashi Yamamoto | Professor Hisashi Yamamoto is chairman of the Molecular Catalysis Center at Chubu University, Japan, Emeritus Professor at the University of Chicago, USA, and Emeritus Professor at Nagoya University, Japan. He is interested in the area of chiral Brønsted acid catalysts, N-Nitroso Aldol (N-NA), and O-Nitroso Aldol reactions. |
Liu-Zhu Gong | Liu-Zhu Gong is currently a Changjiang Scholar Professor of organic chemistry at the University of Science and Technology of China. His current research interest is focused on the organo- and transition metal-catalyzed asymmetric synthesis and total synthesis of natural products. |
The communications and feature articles in this web collection cover important up-to-date information on organocatalysis, and sketch the fruitful development of this exciting field. In particular, the major contributions originated from (1) enamine and iminium catalysis; (2) SOMO and radical enamine catalysis; (3) amine, DMAP and phosphine catalysis; (4) carbene-catalysis, ketone and iminium salt catalysis; (5) organocatalysis using guanidine, amidine and Cinchona alkaloids; (6) organocatalysis with Brønsted acids, thiourea and peptides; and (7) phase-transfer catalysis. In addition, several one-pot multi-step procedures lead to highly functionalized products of wide synthetic applicability. The articles in this issue demonstrate a high, yet sophisticated level of activity in addition to the scope and limitations of this promising field. Accordingly, the readers will enjoy reading the most recent and exciting findings in the current organocatalytic field.
This journal is © The Royal Society of Chemistry 2012 |