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Cofactors and Coenzymes01:24

Cofactors and Coenzymes

Enzymes are proteins made of amino acids. The functional group of each constituent amino acid catalyzes a wide variety of chemical reactions via ionic interactions or acid-base reactions. However, amino acids cannot catalyze oxidation-reduction and group transfer reactions and need to be aided by non-protein components called cofactors. Cofactors are also referred to as the chemical teeth of an enzyme.
Cofactors can be metallic ions or organic molecules called coenzymes. These types of helper...
Cofactors and Coenzymes01:27

Cofactors and Coenzymes

Enzymes require additional components for proper function. There are two such classes of molecules: cofactors and coenzymes. Cofactors are metallic ions and coenzymes are non-protein organic molecules. Both of these types of helper molecule can be tightly bound to the enzyme or bound only when the substrate binds.
Cofactors and Coenzymes01:27

Cofactors and Coenzymes

Enzymes require additional components for proper function. There are two such classes of molecules: cofactors and coenzymes. Cofactors are metallic ions and coenzymes are non-protein organic molecules. Both of these types of helper molecule can be tightly bound to the enzyme or bound only when the substrate binds.
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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...
Heterogeneous Catalysis01:22

Heterogeneous Catalysis

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...
Introduction to Mechanisms of Enzyme Catalysis01:13

Introduction to Mechanisms of Enzyme Catalysis

For many years, scientists thought that enzyme-substrate binding took place in a simple "lock-and-key" fashion. This model stated that the enzyme and substrate fit together perfectly in one instantaneous step. However, current research supports a more refined view scientists call induced fit. The induced-fit model expands upon the lock-and-key model by describing a more dynamic interaction between enzyme and substrate. As the enzyme and substrate come together, their interaction causes a mild...

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Updated: May 28, 2026

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)
08:25

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)

Published on: January 17, 2020

"コファクター"制御されたエナチオセレクティブ触媒.

Paweł Dydio1, Christophe Rubay, Tendai Gadzikwa

  • 1Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Amsterdam, The Netherlands.

Journal of the American Chemical Society
|October 4, 2011
PubMed
まとめ
この要約は機械生成です。

新しいアキラルロジウム複合体は,小さなゲストを結合するとキラルになり,非対称な触媒を可能にします. 最高のゲスト分子は,最大99%のエナチオ選択性を持つ水素化触媒を生成しました.

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Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
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Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy

Published on: November 9, 2019

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues
12:07

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues

Published on: November 22, 2014

関連する実験動画

Last Updated: May 28, 2026

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)
08:25

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)

Published on: January 17, 2020

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
07:36

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy

Published on: November 9, 2019

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues
12:07

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues

Published on: November 22, 2014

科学分野:

  • 有機金属化学 有機金属化学
  • アシンメトリック・カタリシス
  • 超分子化学 超分子化学

背景:

  • アキラルの触媒は,化学反応において,通常,エナチオセレクティブ性が欠けている.
  • チラルの触媒は,エナティオメリカルに純粋な化合物を合成するために不可欠です.
  • 触媒のキラリティを調整できる触媒の設計は大きな課題です.

研究 の 目的:

  • アキラルロジウム複合体を開発し,非対称な触媒を可能にする.
  • キラルアニオンゲスト (共因子) がキラル性を誘発するために使用されることを調査する.
  • 水素化反応における高いエナチオ選択性のためのコファクター選択を最適化するために.

主な方法:

  • ゲスト結合部位を持つアキラルビスフォスフィンロジウム複合体の合成.
  • キラルアニオンゲスト (コファクター) のライブラリのスクリーニング.
  • 非対称な水素化反応における生成されたキラル触媒の評価.

主要な成果:

  • ロジウム複合体は,キラル共因子を認識して結合し,キラル化しました.
  • 最高のコファクターを使用して形成された水素化触媒は,高いエナチオ選択性 (最大99% ee) を達成しました.
  • 競争実験で,最適のコファクタが混合物でも触媒を優位にすることが示されました.

結論:

  • アキラルロジウム複合体は,ゲスト結合によってキラル化され,非対称な触媒を可能にすることができる.
  • 適切なキラルコファクターの選択は,高いエナチオセレクティビティを達成するために非常に重要です.
  • このシステムは,調節可能な非対称な水素化触媒の開発に多岐にわたるアプローチを提供します.