![New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B](https://pubs.rsc.org/image/article/2019/NJ/c8nj06451b/c8nj06451b-s5_hi-res.gif)
New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B
New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing)
![Chiral Bifunctional Thiosquaramides as Organocatalysts in the Synthesis of Enantioenriched 3,3‐Disubstituted Oxindoles - Rodríguez‐Ferrer - 2019 - European Journal of Organic Chemistry - Wiley Online Library Chiral Bifunctional Thiosquaramides as Organocatalysts in the Synthesis of Enantioenriched 3,3‐Disubstituted Oxindoles - Rodríguez‐Ferrer - 2019 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/4b914381-9dba-4c16-ad33-f7e55b16203b/ejoc201901327-fig-0001-m.jpg)
Chiral Bifunctional Thiosquaramides as Organocatalysts in the Synthesis of Enantioenriched 3,3‐Disubstituted Oxindoles - Rodríguez‐Ferrer - 2019 - European Journal of Organic Chemistry - Wiley Online Library
![Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.0c02081/asset/images/large/ja0c02081_0001.jpeg)
Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society
![Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.0c02081/asset/images/large/ja0c02081_0009.jpeg)
Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society
![Molecules | Free Full-Text | Recent Advances in Asymmetric Synthesis of Pyrrolidine-Based Organocatalysts and Their Application: A 15-Year Update Molecules | Free Full-Text | Recent Advances in Asymmetric Synthesis of Pyrrolidine-Based Organocatalysts and Their Application: A 15-Year Update](https://www.mdpi.com/molecules/molecules-28-02234/article_deploy/html/images/molecules-28-02234-g001-550.jpg)
Molecules | Free Full-Text | Recent Advances in Asymmetric Synthesis of Pyrrolidine-Based Organocatalysts and Their Application: A 15-Year Update
![Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes | Journal of the American Chemical Society Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.7b01115/asset/images/medium/ja-2017-01115p_0003.gif)
Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes | Journal of the American Chemical Society
![Dicyclopentyl Dithiosquarate as an Intermediate for the Synthesis of Thiosquaramides | Organic Letters Dicyclopentyl Dithiosquarate as an Intermediate for the Synthesis of Thiosquaramides | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.7b03549/asset/images/medium/ol-2017-03549t_0006.gif)
Dicyclopentyl Dithiosquarate as an Intermediate for the Synthesis of Thiosquaramides | Organic Letters
![Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes | Journal of the American Chemical Society Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.7b01115/asset/images/large/ja-2017-01115p_0005.jpeg)
Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes | Journal of the American Chemical Society
![Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.0c02081/asset/images/medium/ja0c02081_0010.gif)
Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society
![New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B](https://pubs.rsc.org/image/article/2019/NJ/c8nj06451b/c8nj06451b-s1_hi-res.gif)
New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B
![Optimised geometries and schematic structures of binaphthyl-cinchona... | Download Scientific Diagram Optimised geometries and schematic structures of binaphthyl-cinchona... | Download Scientific Diagram](https://www.researchgate.net/publication/331931841/figure/fig1/AS:738874909265930@1553172914850/Optimised-geometries-and-schematic-structures-of-binaphthyl-cinchona-thiosquaramide-1b.jpg)
Optimised geometries and schematic structures of binaphthyl-cinchona... | Download Scientific Diagram
![Dicyclopentyl Dithiosquarate as an Intermediate for the Synthesis of Thiosquaramides | Organic Letters Dicyclopentyl Dithiosquarate as an Intermediate for the Synthesis of Thiosquaramides | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.7b03549/asset/images/medium/ol-2017-03549t_0002.gif)
Dicyclopentyl Dithiosquarate as an Intermediate for the Synthesis of Thiosquaramides | Organic Letters
Dicyclopentyl Dithiosquarate as an Intermediate for the Synthesis of Thiosquaramides | Organic Letters
![New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B](https://pubs.rsc.org/image/article/2019/NJ/c8nj06451b/c8nj06451b-u5_hi-res.gif)
New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B
![Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.0c02081/asset/images/large/ja0c02081_0008.jpeg)
Thiosquaramide-Based Supramolecular Polymers: Aromaticity Gain in a Switched Mode of Self-Assembly | Journal of the American Chemical Society
![New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B](https://pubs.rsc.org/image/article/2019/NJ/c8nj06451b/c8nj06451b-s4_hi-res.gif)
New enantiopure binaphthyl-cinchona thiosquaramides: synthesis and application for enantioselective organocatalysis - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C8NJ06451B
![PDF) Comparison of Cinchona Catalysts Containing Ethyl or Vinyl or Ethynyl Group at Their Quinuclidine Ring PDF) Comparison of Cinchona Catalysts Containing Ethyl or Vinyl or Ethynyl Group at Their Quinuclidine Ring](https://i1.rgstatic.net/publication/335901949_Comparison_of_Cinchona_Catalysts_Containing_Ethyl_or_Vinyl_or_Ethynyl_Group_at_Their_Quinuclidine_Ring/links/5d82dce0299bf1996f77599f/largepreview.png)
PDF) Comparison of Cinchona Catalysts Containing Ethyl or Vinyl or Ethynyl Group at Their Quinuclidine Ring
![Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes | Journal of the American Chemical Society Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.7b01115/asset/images/medium/ja-2017-01115p_0007.gif)
Development of Chiral, Bifunctional Thiosquaramides: Enantioselective Michael Additions of Barbituric Acids to Nitroalkenes | Journal of the American Chemical Society
![Cytotoxicity of cinchona alkaloid organocatalysts against MES-SA and MES-SA/Dx5 multidrug-resistant uterine sarcoma cell lines - ScienceDirect Cytotoxicity of cinchona alkaloid organocatalysts against MES-SA and MES-SA/Dx5 multidrug-resistant uterine sarcoma cell lines - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0968089622002474-ga1.jpg)