Artificial metalloenzymes: reaction scope and optimization strategies

F Schwizer, Y Okamoto, T Heinisch, Y Gu… - Chemical …, 2018 - ACS Publications
The incorporation of a synthetic, catalytically competent metallocofactor into a protein
scaffold to generate an artificial metalloenzyme (ArM) has been explored since the late …

The golden age of transfer hydrogenation

D Wang, D Astruc - Chemical reviews, 2015 - ACS Publications
Hydrogenation is one of the most fundamental transformations in organic synthesis, and its
industrial applications span from fine chemicals to pharmaceuticals synthesis. 1− 3 Direct …

Asymmetric construction of stereogenic carbon centers featuring a trifluoromethyl group from prochiral trifluoromethylated substrates

J Nie, HC Guo, D Cahard, JA Ma - Chemical reviews, 2011 - ACS Publications
Organofluorine chemistry is an area of tremendous expansion. 1 The field of applications is
impressively wide in scope and has the potential to concern all fields of society. Indeed …

Deactivation in homogeneous transition metal catalysis: causes, avoidance, and cure

RH Crabtree - Chemical reviews, 2015 - ACS Publications
Deactivation leads to loss of catalyst activity or selectivity with increasing reaction time, but
has attracted less academic attention in homogeneous catalysis than is justified by its …

Asymmetric transfer hydrogenation of ketones with bifunctional transition metal-based molecular catalysts

T Ikariya, AJ Blacker - Accounts of chemical research, 2007 - ACS Publications
Recent development of conceptually new chiral bifunctional transition metal based catalysts
for asymmetric reductive transformations is described. The chiral bifunctional molecular …

Asymmetric transfer hydrogenation: chiral ligands and applications

S Gladiali, E Alberico - Chemical Society Reviews, 2006 - pubs.rsc.org
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 …

Mechanism of asymmetric hydrogenation of ketones catalyzed by BINAP/1, 2-diamine− ruthenium (II) complexes

CA Sandoval, T Ohkuma, K Muñiz… - Journal of the American …, 2003 - ACS Publications
Asymmetric hydrogenation of acetophenone with trans-RuH (η1-BH4)[(S)-tolbinap][(S, S)-
dpen](TolBINAP= 2, 2 '-bis (di-4-tolylphosphino)-1, 1 '-binaphthyl; DPEN= 1, 2 …

Functionalized imidazolium salts for task-specific ionic liquids and their applications

S Lee - Chemical Communications, 2006 - pubs.rsc.org
Recent developments in task specifically functionalized imidazolium salts, which can be
used for specific tasks ranging from catalysts recycling, supports for organic synthesis …

Broader, greener, and more efficient: Recent advances in asymmetric transfer hydrogenation

C Wang, X Wu, J **ao - Chemistry–An Asian Journal, 2008 - Wiley Online Library
Asymmetric transfer hydrogenation has become a practically useful tool in reduction
chemistry in the last decade or so. This was largely triggered by the seminal work of Noyori …

A class of ruthenium (II) catalyst for asymmetric transfer hydrogenations of ketones

AM Hayes, DJ Morris, GJ Clarkson… - Journal of the American …, 2005 - ACS Publications
Ruthenium dimer 6 (readily available in two steps from TsDPEN) is converted directly to
monomeric asymmetric transfer hydrogenation catalyst 3 in situ under the conditions …