![A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents | Science A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents | Science](https://www.science.org/cms/10.1126/science.aaf6123/asset/137716f1-680a-496e-912c-bd58cd8256f5/assets/graphic/352_801_f3.jpeg)
A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents | Science
![Nickel-Catalyzed Reductive Arylation of Redox Active Esters for the Synthesis of α-Aryl Nitriles – Role of a Chlorosilane Additive | Catalysis | ChemRxiv | Cambridge Open Engage Nickel-Catalyzed Reductive Arylation of Redox Active Esters for the Synthesis of α-Aryl Nitriles – Role of a Chlorosilane Additive | Catalysis | ChemRxiv | Cambridge Open Engage](https://chemrxiv.org/engage/api-gateway/chemrxiv/assets/orp/resource/item/60c757fc702a9b30b718cbe2/largeThumb/nickel-catalyzed-reductive-arylation-of-redox-active-esters-for-the-synthesis-of-aryl-nitriles-role-of-a-chlorosilane-additive.jpg)
Nickel-Catalyzed Reductive Arylation of Redox Active Esters for the Synthesis of α-Aryl Nitriles – Role of a Chlorosilane Additive | Catalysis | ChemRxiv | Cambridge Open Engage
![Decarboxylative Thiolation of Redox-Active Esters to Thioesters by Merging Photoredox and Copper Catalysis | Organic Letters Decarboxylative Thiolation of Redox-Active Esters to Thioesters by Merging Photoredox and Copper Catalysis | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.0c01180/asset/images/medium/ol0c01180_0001.gif)
Decarboxylative Thiolation of Redox-Active Esters to Thioesters by Merging Photoredox and Copper Catalysis | Organic Letters
![Reactions of copper amine complexes with a redox-active ester Variation... | Download Scientific Diagram Reactions of copper amine complexes with a redox-active ester Variation... | Download Scientific Diagram](https://www.researchgate.net/publication/322990660/figure/fig4/AS:941138169053188@1601396233785/Reactions-of-copper-amine-complexes-with-a-redox-active-ester-Variation-of-yield-with.jpg)
Reactions of copper amine complexes with a redox-active ester Variation... | Download Scientific Diagram
![Site- and Stereoselective Reductive Alkylalkynylation of Alkynes using Redox-Active Esters as Alkyl Group Donors | Organic Chemistry | ChemRxiv | Cambridge Open Engage Site- and Stereoselective Reductive Alkylalkynylation of Alkynes using Redox-Active Esters as Alkyl Group Donors | Organic Chemistry | ChemRxiv | Cambridge Open Engage](https://chemrxiv.org/engage/api-gateway/chemrxiv/assets/orp/resource/item/60c751e6567dfe16beec5b4a/largeThumb/site-and-stereoselective-reductive-alkylalkynylation-of-alkynes-using-redox-active-esters-as-alkyl-group-donors.jpg)
Site- and Stereoselective Reductive Alkylalkynylation of Alkynes using Redox-Active Esters as Alkyl Group Donors | Organic Chemistry | ChemRxiv | Cambridge Open Engage
![Decarboxylative thiolation of redox-active esters to free thiols and further diversification | Nature Communications Decarboxylative thiolation of redox-active esters to free thiols and further diversification | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-020-19195-w/MediaObjects/41467_2020_19195_Fig1_HTML.png)
Decarboxylative thiolation of redox-active esters to free thiols and further diversification | Nature Communications
![a Some commonly used reagents for active ester preparation. b Active... | Download Scientific Diagram a Some commonly used reagents for active ester preparation. b Active... | Download Scientific Diagram](https://www.researchgate.net/publication/321339947/figure/fig8/AS:960327218905101@1605971259291/a-Some-commonly-used-reagents-for-active-ester-preparation-b-Active-ester-mediated.gif)
a Some commonly used reagents for active ester preparation. b Active... | Download Scientific Diagram
![Utilization of C(sp3)‐Carboxylic Acids and Their Redox‐Active Esters in Decarboxylative Carbon−Carbon Bond Formation - ScienceDirect Utilization of C(sp3)‐Carboxylic Acids and Their Redox‐Active Esters in Decarboxylative Carbon−Carbon Bond Formation - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1615415022010019-adsc202100314-toc-0001.jpg)
Utilization of C(sp3)‐Carboxylic Acids and Their Redox‐Active Esters in Decarboxylative Carbon−Carbon Bond Formation - ScienceDirect
![Enzymatic synthesis of activated esters and their subsequent use in enzyme-based peptide synthesis - ScienceDirect Enzymatic synthesis of activated esters and their subsequent use in enzyme-based peptide synthesis - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1381117711000968-fx1.jpg)
Enzymatic synthesis of activated esters and their subsequent use in enzyme-based peptide synthesis - ScienceDirect
![N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions - Murarka - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions - Murarka - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/6f4a10bb-8c94-47d7-85f3-a43fe5871d3e/adsc201701615-fig-5024-m.jpg)
N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions - Murarka - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library
![Nickel‐Catalyzed Cross‐Coupling of Redox‐Active Esters with Boronic Acids - Wang - 2016 - Angewandte Chemie International Edition - Wiley Online Library Nickel‐Catalyzed Cross‐Coupling of Redox‐Active Esters with Boronic Acids - Wang - 2016 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/21f0b0af-2530-4958-80aa-fe8fa1379e21/anie201605463-fig-0001-m.jpg)
Nickel‐Catalyzed Cross‐Coupling of Redox‐Active Esters with Boronic Acids - Wang - 2016 - Angewandte Chemie International Edition - Wiley Online Library
Visible-light induced decarboxylative coupling of redox-active esters with disulfides to construct C–S bonds - Chemical Communications (RSC Publishing)
![Decarboxylative thiolation of redox-active esters to free thiols and further diversification | Nature Communications Decarboxylative thiolation of redox-active esters to free thiols and further diversification | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-020-19195-w/MediaObjects/41467_2020_19195_Fig4_HTML.png)
Decarboxylative thiolation of redox-active esters to free thiols and further diversification | Nature Communications
![N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions - Murarka - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions - Murarka - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/0f325263-44ca-4fd5-bee4-930ab1e4856f/adsc201701615-fig-5035-m.jpg)
N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions - Murarka - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library
Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis - Organic Chemistry Frontiers (RSC Publishing)
![N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions - Murarka - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library N‐(Acyloxy)phthalimides as Redox‐Active Esters in Cross‐Coupling Reactions - Murarka - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/602ae32e-b380-41e8-85f6-9f9ba88417d8/adsc201701615-fig-5001-m.jpg)