Nontoxic, nonvolatile, and highly efficient osmium catalysts for asymmetric dihydroxylation of alkenes and application to one mol-scale synthesis of an anticancer drug, camptothecin intermediate†
Abstract
Novel
* Corresponding authors
a
Department of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
E-mail:
shu_kobayashi@chem.s.u-tokyo.ac.jp
Fax: +81 3 5841 4790
Tel: +81 3 5684 0634
b Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
c Division of Environmental Research, EcoTopia Science Institute, Nagoya University, Nagoya 464-8603, Japan
d Division of Quantum Science and Energy Engineering, Department of Materials, Physics and Energy Engineering, Nagoya University, Nagoya 464-8603, Japan
Novel
R. Akiyama, N. Matsuki, H. Nomura, H. Yoshida, T. Yoshida and S. Kobayashi, RSC Adv., 2012, 2, 7456 DOI: 10.1039/C2RA21123H
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