R Noyori, T Ohkuma - Angewandte Chemie International …, 2001 - Wiley Online Library
Hydrogenation is a core technology in chemical synthesis. High rates and selectivities are attainable only by the coordination of structurally well‐designed catalysts and suitable …
M Nishio - Physical Chemistry Chemical Physics, 2011 - pubs.rsc.org
The CH/π hydrogen bond is an attractive molecular force occurring between a soft acid and a soft base. Contribution from the dispersion energy is important in typical cases where …
The first supplement to the three volume reference work" Comprehensive Asymmetric Catalysis" critically reviews new developments to the hottest topics in the field written by …
SE Clapham, A Hadzovic, RH Morris - Coordination Chemistry Reviews, 2004 - Elsevier
The catalytic cycles for the H2-hydrogenation (H) and transfer hydrogenation (T) of C O and C N bonds catalyzed by over 100 ruthenium hydride complexes in organic and …
Hydrogen transfer reduction processes are attracting increasing interest from synthetic chemists in view of their operational simplicity and high selectivity. In this tutorial review the …
O Takahashi, Y Kohno, M Nishio - Chemical reviews, 2010 - ACS Publications
Organic chemists tend to consider the conformation of compounds as a consequence of repulsive steric interactions. In other words,“the steric effect” means “repulsive” in many …
B Zhao, Z Han, K Ding - Angewandte Chemie International …, 2013 - Wiley Online Library
The organometallic approach is one of the most active topics in catalysis. The application of NH functionality in organometallic catalysis has become an important and attractive concept …
The start of the development of catalysts for asymmetric hydrogenation was the concept of replacing the triphenylphosphane ligand of the Wilkinson catalyst with a chiral ligand. With …
M Nishio, Y Umezawa, K Honda, S Tsuboyama… - …, 2009 - pubs.rsc.org
This treatise is an update to a preceding highlight (CH/π hydrogen bonds in crystals) published in this journal 5 years ago (M. Nishio, CrystEngComm, 2004, 6, 130–156). After …