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Related Concept Videos

Heterogeneous Catalysis01:22

Heterogeneous Catalysis

41
Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...
41
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide02:44

Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

13.2K
Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
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Properties of Transition Metals02:58

Properties of Transition Metals

30.4K
Transition metals are defined as those elements that have partially filled d orbitals. As shown in Figure 1, the d-block elements in groups 3–12 are transition elements. The f-block elements, also called inner transition metals (the lanthanides and actinides), also meet this criterion because the d orbital is partially occupied before the f orbitals.
30.4K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

4.0K
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
4.0K
Oxidation-Reduction Reactions03:11

Oxidation-Reduction Reactions

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Oxidation–Reduction Reactions
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Oxidation of Alcohols02:37

Oxidation of Alcohols

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In this lesson, the oxidation of alcohols is discussed in depth. The various reagents used for oxidation of primary and secondary alcohols are detailed, and their mechanism of action is provided.
The process of oxidation in a chemical reaction is observed in any of the three forms:
17.2K

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Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs
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Asymmetric Homogeneous Oxidation Reactions Catalyzed by First-Row Transition Metal Complexes.

Geeta Devi Yadav1,2, Deepa Uppal1, Priyanka Jhajharia3

  • 1Department of Chemistry, University of Delhi, New Delhi, India.

Chirality
|March 5, 2026
PubMed
Summary
This summary is machine-generated.

This review summarizes asymmetric homogeneous oxidation reactions using first-row transition metal complexes. It highlights chiral catalyst performance, focusing on ligands, metals, and reaction conditions for efficient oxidation catalysis.

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Area of Science:

  • Catalysis
  • Organic Chemistry
  • Materials Science

Background:

  • Asymmetric homogeneous oxidation reactions are crucial for synthesizing chiral molecules.
  • First-row transition metal complexes offer cost-effective and sustainable catalytic solutions.
  • Understanding catalyst performance requires analyzing key factors like ligand structure and reaction conditions.

Purpose of the Study:

  • To review asymmetric homogeneous oxidation reactions catalyzed by first-row transition metal complexes.
  • To analyze the relationship between chiral catalyst performance and key factors.
  • To provide a comprehensive overview of homogeneous asymmetric oxidation catalysts.

Main Methods:

  • Literature review of asymmetric homogeneous oxidation reactions.
  • Focus on catalytic systems involving first-row transition metals and chiral ligands.
  • Analysis of various oxidants including hydrogen peroxide, molecular oxygen, and tert-butyl hydroperoxide.

Main Results:

  • Manganese complexes are extensively used for epoxidation, hydroxylation, and oxidative kinetic resolution.
  • Various first-row transition metals (Ti, Cr, Mn, Fe, Co, V) and chiral ligands are employed.
  • Diverse oxidation reactions are achieved, including epoxidation, sulfoxidation, and hydroxylation.

Conclusions:

  • First-row transition metal complexes are effective homogeneous catalysts for asymmetric oxidation.
  • Chiral ligand design and reaction parameters significantly influence catalyst performance.
  • This review enhances the understanding of homogeneous asymmetric oxidation catalysis.