Catalytic Asymmetric Oxygenations with the Environmentally Benign Oxidants H2O2 and O2.
349
TL;DR: An overview of catalyst systems capable of conducting asymmetric oxygenative transformations of organic molecules and, in line with the major trend to sustainability, relying on green oxidants H2O2 and O2 as the ultimate oxygen source is given.
read more
Abstract: The discovery of simple and efficient catalyst systems for the asymmetric oxofunctionalization of hydrocarbons is a challenging task of catalytic chemistry. In this paper, we give an overview of catalyst systems capable of conducting asymmetric oxygenative transformations of organic molecules and, in line with the major trend to sustainability, relying on green oxidants H2O2 and O2 as the ultimate oxygen source. The full historical period of asymmetric oxidation catalysis (1970 to the present day) is covered; both transition-metal-based and organocatalytic systems are considered. The focus of this review is the catalytic properties of the existing catalyst systems, in particular stereoselectivity, activity, efficiency, and synthetic outlook. At the same time, mechanistic peculiarities of stereoselective oxygen transfer are given attention.
read more
Chat with Paper
AI Agents for this Paper
Find similar papers on Google Scholar, PubMed and Arxiv
Write a critical review of this paper
Analyze citations of this paper to find unaddressed research gaps
Citations
Recent advances in titanium-based catalysts with N, O-donor ligands: synthetic approach and catalytic applications
Sonal Verma,Sunita Arya,Robina Aman +2 more
Excellent Catalytic Performances of a Au/C–CuO Binary System in the Selective Oxidation of Benzylamines to Imines under Atmospheric Oxygen
Yuki Yamamoto,Miyuto Ota,Shintaro Kodama,Michio Ueshima,Akihiro Nomoto,Akiya Ogawa,Mitsunori Furuya,Kiminori Kawakami +7 more
TL;DR: A novel Au/C–CuO binary system catalyzes the selective oxidation of benzylamines to imines under atmospheric oxygen, achieving up to 100% yields with high durability and recyclability, and successfully synthesizing N-containing functional molecules on a large scale.
Enantioselective Epoxidation of β,β-Disubstituted Enamides with a Manganese Catalyst and Aqueous Hydrogen Peroxide.
TL;DR: Amides are disclosed as key functional groups to enable high enantioselectivity in epoxidation of β,β-disubstituted enamides with aqueous hydrogen peroxide and a novel manganese catalyst.
Palladium‐Catalyzed Enantioselective Hydrofunctionalization of Alkenes: Recent Advances
08 Sep 2023
TL;DR: Palladium-catalyzed enantioselective hydrofunctionalization of alkenes is a powerful method to synthesize enantioenriched molecules.
Peroxide-Driven Hydroxylation of Small Alkanes Catalyzedby an Artificial P450BM3 Peroxygenase System
TL;DR: The substitution of the highly conserved T268 with amino acids having hydrophobic side chains was identified to play critical roles in improving the hydroxylation activity of the DFSM-facilitated P450BM3 peroxygenase system, which is distinct from NADPH-dependent P450 enzymes.
References
•Book
Green Chemistry: Theory and Practice
Paul T. Anastas,John C. Warner +1 more
- 01 Jan 1998
TL;DR: Green Chemistry: What is green chemistry? as discussed by the authors presents the principles of green chemistry and evaluates the impact of chemistry on the environment. But, it is not a complete overview of all of the issues involved in green chemistry.
8.7K
The atom economy--a search for synthetic efficiency
TL;DR: Transition metal-catalyzed methods that are both selective and economical for formation of cyclic structures, of great interest for biological purposes, represent an important starting point for this long-term goal.
4.4K
•Book
Comprehensive asymmetric catalysis
Eric N. Jacobsen,Andreas Pfaltz,尚 山本 +2 more
- 01 Jan 1999
TL;DR: Ohkuma et al. as mentioned in this paper proposed an asymmetric Dihydroxylation process for carbon-Carbon double bonds and showed that it can be used for allylation of C=O.
3.9K
Origins, Current Status, and Future Challenges of Green Chemistry†
TL;DR: The origins and basis of green chemistry chart a course for achieving environmental and economic prosperity inherent in a sustainable world.
2.1K
Comprehensive Asymmetric Catalysis I–III
Eric N. Jacobsen,Andreas Pfaltz,Hisashi Yamamoto +2 more
- 01 Jan 1999
1.5K