![Full article: Urban Oligarchy and Dissolutioned Voters: The End of Monastic Rule in Reading, 1350-1600 Full article: Urban Oligarchy and Dissolutioned Voters: The End of Monastic Rule in Reading, 1350-1600](https://www.tandfonline.com/cms/asset/08be8786-09fd-4769-9379-79666d47e344/rfcs_a_1661556_f0007_b.gif)
Full article: Urban Oligarchy and Dissolutioned Voters: The End of Monastic Rule in Reading, 1350-1600
![A2[MX4] Copper(II) Pyridinium Salts. From Ionic Liquids to Layered Solids to Liquid Crystals | Chemistry of Materials A2[MX4] Copper(II) Pyridinium Salts. From Ionic Liquids to Layered Solids to Liquid Crystals | Chemistry of Materials](https://pubs.acs.org/cms/10.1021/cm000804d/asset/images/medium/cm000804df1.gif)
A2[MX4] Copper(II) Pyridinium Salts. From Ionic Liquids to Layered Solids to Liquid Crystals | Chemistry of Materials
![Synthetic applications of type II intramolecular cycloadditions - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D0CS00365D Synthetic applications of type II intramolecular cycloadditions - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D0CS00365D](https://pubs.rsc.org/image/article/2020/CS/d0cs00365d/d0cs00365d-s2_hi-res.gif)
Synthetic applications of type II intramolecular cycloadditions - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D0CS00365D
![A2[MX4] Copper(II) Pyridinium Salts. From Ionic Liquids to Layered Solids to Liquid Crystals | Chemistry of Materials A2[MX4] Copper(II) Pyridinium Salts. From Ionic Liquids to Layered Solids to Liquid Crystals | Chemistry of Materials](https://pubs.acs.org/cms/10.1021/cm000804d/asset/images/medium/cm000804df00008.gif)
A2[MX4] Copper(II) Pyridinium Salts. From Ionic Liquids to Layered Solids to Liquid Crystals | Chemistry of Materials
![On the Release of Hydrogen from the S−H groups in the Formation of Self-Assembled Monolayers of Thiols | Langmuir On the Release of Hydrogen from the S−H groups in the Formation of Self-Assembled Monolayers of Thiols | Langmuir](https://pubs.acs.org/cms/10.1021/la902168u/asset/images/large/la-2009-02168u_0005.jpeg)
On the Release of Hydrogen from the S−H groups in the Formation of Self-Assembled Monolayers of Thiols | Langmuir
![Single‐Atom Nanozymes for Biomedical Applications: Recent Advances and Challenges - Tang - 2022 - Chemistry – An Asian Journal - Wiley Online Library Single‐Atom Nanozymes for Biomedical Applications: Recent Advances and Challenges - Tang - 2022 - Chemistry – An Asian Journal - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/53557bd5-6db9-4080-80bf-0e5331d99f2b/asia202101422-toc-0001-m.jpg)
Single‐Atom Nanozymes for Biomedical Applications: Recent Advances and Challenges - Tang - 2022 - Chemistry – An Asian Journal - Wiley Online Library
![Conformational Preferences of Allene Ketones in Lewis Base Catalysis: Synthesis of 4H‐Pyrans and 3,4‐Dihydro‐2H‐pyrans via α‐Regioselective [4+2] Annulations of γ‐Substituted Allene Ketones and Activated Alkenes - Hou - 2021 - Asian Journal Conformational Preferences of Allene Ketones in Lewis Base Catalysis: Synthesis of 4H‐Pyrans and 3,4‐Dihydro‐2H‐pyrans via α‐Regioselective [4+2] Annulations of γ‐Substituted Allene Ketones and Activated Alkenes - Hou - 2021 - Asian Journal](https://onlinelibrary.wiley.com/cms/asset/23891b2b-157f-49d7-b63f-4eb2de643e34/ajoc202100523-fig-5001-m.jpg)
Conformational Preferences of Allene Ketones in Lewis Base Catalysis: Synthesis of 4H‐Pyrans and 3,4‐Dihydro‐2H‐pyrans via α‐Regioselective [4+2] Annulations of γ‐Substituted Allene Ketones and Activated Alkenes - Hou - 2021 - Asian Journal
![Site-selective modification of peptide backbones - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/D1QO00892G Site-selective modification of peptide backbones - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/D1QO00892G](https://pubs.rsc.org/image/article/2021/QO/d1qo00892g/d1qo00892g-s33.gif)
Site-selective modification of peptide backbones - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/D1QO00892G
![Stille Cross-Coupling Reactions of Alkenylstannanes with Alkenyl Iodides Mediated by Copper(I) Thiophene-2-carboxylate: A Density Functional Study | Organometallics Stille Cross-Coupling Reactions of Alkenylstannanes with Alkenyl Iodides Mediated by Copper(I) Thiophene-2-carboxylate: A Density Functional Study | Organometallics](https://pubs.acs.org/cms/10.1021/om100304t/asset/images/large/om-2010-00304t_0004.jpeg)