Ring openings of lactone and ring contractions of lactide by frustrated Lewis pairs - Dalton Transactions (RSC Publishing)
![Size range of lactone rings produced by TE domains. The lactone ring of... | Download Scientific Diagram Size range of lactone rings produced by TE domains. The lactone ring of... | Download Scientific Diagram](https://www.researchgate.net/publication/354037390/figure/fig5/AS:1060260529844225@1629797217672/Size-range-of-lactone-rings-produced-by-TE-domains-The-lactone-ring-of-obafluorin-16.png)
Size range of lactone rings produced by TE domains. The lactone ring of... | Download Scientific Diagram
![the Sugar and Lactone Ring Structure-Activity Relationships for the Hypertensinogenic Activity of Ouabain : Role of | Semantic Scholar the Sugar and Lactone Ring Structure-Activity Relationships for the Hypertensinogenic Activity of Ouabain : Role of | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/9c9c39952a2f3defc861fc6a9f8dd5960a1c7d0c/3-Figure1-1.png)
the Sugar and Lactone Ring Structure-Activity Relationships for the Hypertensinogenic Activity of Ouabain : Role of | Semantic Scholar
![Mild and Chemoselective Lactone Ring-Opening with (TMS)ONa. Mechanistic Studies and Application to Sweroside Derivatives | The Journal of Organic Chemistry Mild and Chemoselective Lactone Ring-Opening with (TMS)ONa. Mechanistic Studies and Application to Sweroside Derivatives | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/jo500220h/asset/images/large/jo-2014-00220h_0005.jpeg)
Mild and Chemoselective Lactone Ring-Opening with (TMS)ONa. Mechanistic Studies and Application to Sweroside Derivatives | The Journal of Organic Chemistry
![Organocatalysis applied to the ring‐opening polymerization of β‐lactones: A brief overview - Khalil - 2019 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library Organocatalysis applied to the ring‐opening polymerization of β‐lactones: A brief overview - Khalil - 2019 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/93cd0552-7452-4d03-a676-0c99e7a0ea7b/pola29322-fig-0005-m.jpg)
Organocatalysis applied to the ring‐opening polymerization of β‐lactones: A brief overview - Khalil - 2019 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library
![A thermal lactone ring opening/closing reaction. H-EA=Electron acceptor | Download Scientific Diagram A thermal lactone ring opening/closing reaction. H-EA=Electron acceptor | Download Scientific Diagram](https://www.researchgate.net/publication/264782706/figure/fig1/AS:295850803777548@1447547736877/A-thermal-lactone-ring-opening-closing-reaction-H-EAElectron-acceptor.png)
A thermal lactone ring opening/closing reaction. H-EA=Electron acceptor | Download Scientific Diagram
![Active parts of aflatoxin molecule Key; a -Furan ring, b-lactone ring,... | Download Scientific Diagram Active parts of aflatoxin molecule Key; a -Furan ring, b-lactone ring,... | Download Scientific Diagram](https://www.researchgate.net/publication/354182504/figure/fig1/AS:11431281086097871@1664101974168/Active-parts-of-aflatoxin-molecule-Key-a-Furan-ring-b-lactone-ring-c-cyclopentanone.png)
Active parts of aflatoxin molecule Key; a -Furan ring, b-lactone ring,... | Download Scientific Diagram
![Synthesis of New Camptothecin Analogues with the E‐Lactone Ring Replaced by α,β‐Cyclohexenone - Bacherikov - 2006 - European Journal of Organic Chemistry - Wiley Online Library Synthesis of New Camptothecin Analogues with the E‐Lactone Ring Replaced by α,β‐Cyclohexenone - Bacherikov - 2006 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/28400d84-f561-4a47-b6b5-8f120f058abd/mfig000.gif)
Synthesis of New Camptothecin Analogues with the E‐Lactone Ring Replaced by α,β‐Cyclohexenone - Bacherikov - 2006 - European Journal of Organic Chemistry - Wiley Online Library
![Catalytic Redox Chain Ring Opening of Lactones with Quinones To Synthesize Quinone-Containing Carboxylic Acids | Organic Letters Catalytic Redox Chain Ring Opening of Lactones with Quinones To Synthesize Quinone-Containing Carboxylic Acids | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.9b01672/asset/images/large/ol-2019-01672w_0004.jpeg)
Catalytic Redox Chain Ring Opening of Lactones with Quinones To Synthesize Quinone-Containing Carboxylic Acids | Organic Letters
![Ring-opening polymerization of a five-membered lactone trans-fused to a cyclohexane ring | Polymer Journal Ring-opening polymerization of a five-membered lactone trans-fused to a cyclohexane ring | Polymer Journal](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fpj.2013.70/MediaObjects/41428_2014_Article_BFpj201370_Figb_HTML.jpg)
Ring-opening polymerization of a five-membered lactone trans-fused to a cyclohexane ring | Polymer Journal
![Molecules | Free Full-Text | Lactones 41. Synthesis and Microbial Hydroxylation of Unsaturated Terpenoid Lactones with p-Menthane Ring Systems Molecules | Free Full-Text | Lactones 41. Synthesis and Microbial Hydroxylation of Unsaturated Terpenoid Lactones with p-Menthane Ring Systems](https://www.mdpi.com/molecules/molecules-18-02778/article_deploy/html/images/molecules-18-02778-g001.png)
Molecules | Free Full-Text | Lactones 41. Synthesis and Microbial Hydroxylation of Unsaturated Terpenoid Lactones with p-Menthane Ring Systems
![Lactones: Classification, synthesis, biological activities, and industrial applications - ScienceDirect Lactones: Classification, synthesis, biological activities, and industrial applications - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402021001009-gr1.jpg)