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Articles by Ryosuke Haraguchi
Charge-Enhanced Reactivity of Esters by a Cationic Substituent
Download Hi-Res ImageDownload to MS-PowerPointCite This:Org. Lett. 2024, XXXX, XXX RETURN TO ARTICLES ASAPPREVLetterNEXT Masaaki Sakuma Department of Applied Chemistry, Graduate School of Engineering, Chiba Institute of Technology, 2-17-1 Tsudanuma, Narashino, Chiba 275-0016, Japan and * LEARN ABOUT THESE METRICS Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals.
Synthesis of Pseudo-Glycoside hybrid steroid dimers NMR and X-ray characterization
Introduction Glycosides comprise an important class of secondary metabolites that are present in a wide diversity of marine and terrestrial organisms [1]. Due their wide distribution and extremely varied biological activities, these compounds have remained in the focus of attention for more than one century. Steroid saponins constitute a heavily populated subfamily of glycosides. A high number of steroids isolated from plants occur as glycosides.
Planar-chiral ferrocene-based triazolylidene copper complexes: synthesis, characterization, and catalysis in asymmetric borylation of α,β-unsaturated ester
Planar-chiral ferrocene-based triazolylidene copper complexes: synthesis, characterization, and catalysis in asymmetric borylation of α,β-unsaturated ester† Ryosuke Haraguchi, *a Tatsuro Yamazaki,b Koki Torita,b Tatsuki Itob and Shin-ichi Fukuzawa *b Author affiliations * Corresponding authors a Department of Applied Chemistry, Faculty of Engineering, Chiba Institute of Technology, 2-17-1 Tsudanuma, Narashino, Chiba 275-0016, Japan E-mail: haraguchi.ryosuke@p.chibakoudai.jp b Department of...
Lewis acid-base synergistic catalysis of cationic halogen-bonding-donors with nucleophilic counter anions
Lewis acid–base synergistic catalysis of cationic halogen-bonding-donors with nucleophilic counter anions Cationic halogen-bonding-donors with little or non-coordinating counter anions have attracted great attention as new Lewis acid type organocatalysts. However, these anions cannot function as nucleophilic activation sites due to their low Lewis basicity.
Bulky iodotriazolium tetrafluoroborates as highly active halogen-bonding-donor catalysts
R. Haraguchi, S. Hoshino, M. Sakai, S. Tanazawa, Y. morita, T. Komatsu and S. Fukuzawa, Chem. Commun., 2018, Accepted Manuscript , DOI: 10.1039/C8CC05309J If you are not the author of this article and you wish to reproduce material from it in a third party non-RSC publication you must formally request permission using RightsLink. Go to our Instructions for using RightsLink page for details.
Chiral triazolylidene-Pd-PEPPSI: synthesis, characterization, and application in asymmetric Suzuki-Miyaura cross-coupling
R. Haraguchi, S. Hoshino, T. Yamazaki and S. Fukuzawa, Chem. Commun., 2018, Accepted Manuscript , DOI: 10.1039/C7CC09960F If you are not the author of this article and you wish to reproduce material from it in a third party non-RSC publication you must formally request permission using RightsLink. Go to our Instructions for using RightsLink page for details.
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