![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/4e2d01e8-3cae-4c7d-a6ba-19c3e8334bf2/pola29322-fig-0008-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
![SciELO - Brasil - Synthesis of medium ring and macrocyclic acetylenic lactones by the ring expansion of oxabicycloalkenones Synthesis of medium ring and macrocyclic acetylenic lactones by the ring expansion of oxabicycloalkenones SciELO - Brasil - Synthesis of medium ring and macrocyclic acetylenic lactones by the ring expansion of oxabicycloalkenones Synthesis of medium ring and macrocyclic acetylenic lactones by the ring expansion of oxabicycloalkenones](https://minio.scielo.br/documentstore/1678-4790/jw3PpVVdJrTTVHGyL9tGy6k/602f8298cfc48fdce27c3a7fbf4b40e3e4135a17.gif)
SciELO - Brasil - Synthesis of medium ring and macrocyclic acetylenic lactones by the ring expansion of oxabicycloalkenones Synthesis of medium ring and macrocyclic acetylenic lactones by the ring expansion of oxabicycloalkenones
Ring openings of lactone and ring contractions of lactide by frustrated Lewis pairs - Dalton Transactions (RSC Publishing)
![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/medium/jo-2014-00220h_0005.gif)
Mild and Chemoselective Lactone Ring-Opening with (TMS)ONa. Mechanistic Studies and Application to Sweroside Derivatives | The Journal of Organic Chemistry
![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://pub.mdpi-res.com/molecules/molecules-18-02778/article_deploy/html/images/molecules-18-02778-g001.png?1537156298)
Molecules | Free Full-Text | Lactones 41. Synthesis and Microbial Hydroxylation of Unsaturated Terpenoid Lactones with p-Menthane Ring Systems
![Download Macrolide-antibiotics - Lactone Ring In Azithromycin PNG Image with No Background - PNGkey.com Download Macrolide-antibiotics - Lactone Ring In Azithromycin PNG Image with No Background - PNGkey.com](https://www.pngkey.com/png/full/355-3553610_macrolide-antibiotics-lactone-ring-in-azithromycin.png)
Download Macrolide-antibiotics - Lactone Ring In Azithromycin PNG Image with No Background - PNGkey.com
![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
![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_0011.jpeg)
Mild and Chemoselective Lactone Ring-Opening with (TMS)ONa. Mechanistic Studies and Application to Sweroside Derivatives | The Journal of Organic Chemistry
Structural Basis of the γ-Lactone-Ring Formation in Ascorbic Acid Biosynthesis by the Senescence Marker Protein-30/Gluconolactonase | PLOS ONE
![Biological stains; a handbook on the nature and uses of the dyes employed in the biological laboratory. Stains and staining (Microscopy); Stains and Staining; Dyes. 184 Biological Stains 3. FLUORAN DERIVATIVES Biological stains; a handbook on the nature and uses of the dyes employed in the biological laboratory. Stains and staining (Microscopy); Stains and Staining; Dyes. 184 Biological Stains 3. FLUORAN DERIVATIVES](https://c8.alamy.com/comp/RHM26A/biological-stains-a-handbook-on-the-nature-and-uses-of-the-dyes-employed-in-the-biological-laboratory-stains-and-staining-microscopy-stains-and-staining-dyes-184-biological-stains-3-fluoran-derivatives-fluoran-is-not-a-dye-but-is-a-very-important-compound-in-dye-chemistry-it-is-a-derivative-of-phthalic-anhjdride-and-contains-a-xanthene-ring-five-c-atoms-and-one-o-atom-as-well-as-a-lactone-ring-four-c-atoms-and-one-o-atom-besides-three-benzene-rings-thus-o-the-fluoran-dyes-are-derivatives-of-this-by-the-introduction-of-hydroxyl-groups-into-two-of-the-benzene-rings-at-the-p-RHM26A.jpg)
Biological stains; a handbook on the nature and uses of the dyes employed in the biological laboratory. Stains and staining (Microscopy); Stains and Staining; Dyes. 184 Biological Stains 3. FLUORAN DERIVATIVES
![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)
Lactones: Classification, synthesis, biological activities, and industrial applications - ScienceDirect
![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
![Biosynthesis of ebelactone A: isotopic tracer, advanced precursor and genetic studies reveal a thioesterase-independent cyclization to give a polyketide β-lactone | The Journal of Antibiotics Biosynthesis of ebelactone A: isotopic tracer, advanced precursor and genetic studies reveal a thioesterase-independent cyclization to give a polyketide β-lactone | The Journal of Antibiotics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fja.2013.48/MediaObjects/41429_2013_Article_BFja201348_Fig1_HTML.jpg)