![Effect of Methods and Catalysts on the One-pot Synthesis of Tetrahydropyridine Derivatives: A Mini-Review | Orbital: The Electronic Journal of Chemistry Effect of Methods and Catalysts on the One-pot Synthesis of Tetrahydropyridine Derivatives: A Mini-Review | Orbital: The Electronic Journal of Chemistry](https://periodicos.ufms.br/public/journals/61/article_15581_cover_en_US.png)
Effect of Methods and Catalysts on the One-pot Synthesis of Tetrahydropyridine Derivatives: A Mini-Review | Orbital: The Electronic Journal of Chemistry
![Amphiphilic fluorescent copolymers via one-pot synthesis of RAFT polymerization and multicomponent Biginelli reaction and their cells imaging applications | Journal of Materials Research | Cambridge Core Amphiphilic fluorescent copolymers via one-pot synthesis of RAFT polymerization and multicomponent Biginelli reaction and their cells imaging applications | Journal of Materials Research | Cambridge Core](https://static.cambridge.org/binary/version/id/urn:cambridge.org:id:binary:20190926182337699-0824:S0884291419001638:S0884291419001638_fig7g.jpeg?pub-status=live)
Amphiphilic fluorescent copolymers via one-pot synthesis of RAFT polymerization and multicomponent Biginelli reaction and their cells imaging applications | Journal of Materials Research | Cambridge Core
One-pot quadruple/triple reaction sequence: a useful tool for the synthesis of natural products - Organic & Biomolecular Chemistry (RSC Publishing)
![A facile one-pot synthesis of new functionalized pyrazolone-1,4-dithiafulvene hybrids | Molecular Diversity A facile one-pot synthesis of new functionalized pyrazolone-1,4-dithiafulvene hybrids | Molecular Diversity](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs11030-022-10473-x/MediaObjects/11030_2022_10473_Figa_HTML.png)
A facile one-pot synthesis of new functionalized pyrazolone-1,4-dithiafulvene hybrids | Molecular Diversity
![One‐Pot Synthesis of Cycloocta[b]indole Through Formal [5+3] Cycloaddition Using Donor–Acceptor Cyclopropanes - Okabe - 2019 - European Journal of Organic Chemistry - Wiley Online Library One‐Pot Synthesis of Cycloocta[b]indole Through Formal [5+3] Cycloaddition Using Donor–Acceptor Cyclopropanes - Okabe - 2019 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/dadcdf11-c1cf-437b-ba95-879966dd809b/ejoc201900610-toc-0001-m.png)
One‐Pot Synthesis of Cycloocta[b]indole Through Formal [5+3] Cycloaddition Using Donor–Acceptor Cyclopropanes - Okabe - 2019 - European Journal of Organic Chemistry - Wiley Online Library
One-Pot, Two-Step Synthesis of Imidazo[1,2-a]benzimidazoles via A Multicomponent [4 + 1] Cycloaddition Reaction | ACS Combinatorial Science
An electrochemical tandem reaction: one-pot synthesis of homoallylic alcohols from alcohols in aqueous media - Chemical Communications (RSC Publishing)
![Efficient one-pot synthesis of substituted diphenyl 1, 3-thiazole through multicomponent reaction by using green and efficient Iron-catalyst via Cross-Dehydrogenative Coupling(CDC) | Molecular Diversity Efficient one-pot synthesis of substituted diphenyl 1, 3-thiazole through multicomponent reaction by using green and efficient Iron-catalyst via Cross-Dehydrogenative Coupling(CDC) | Molecular Diversity](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs11030-021-10191-w/MediaObjects/11030_2021_10191_Figa_HTML.png)
Efficient one-pot synthesis of substituted diphenyl 1, 3-thiazole through multicomponent reaction by using green and efficient Iron-catalyst via Cross-Dehydrogenative Coupling(CDC) | Molecular Diversity
![One‐Pot Two‐Step Chemoenzymatic Cascade for the Synthesis of a Bis‐benzofuran Derivative - Mertens - 2019 - European Journal of Organic Chemistry - Wiley Online Library One‐Pot Two‐Step Chemoenzymatic Cascade for the Synthesis of a Bis‐benzofuran Derivative - Mertens - 2019 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/87283789-ca06-4c23-8c00-ae76aee47813/ejoc201900904-toc-0001-m.jpg)
One‐Pot Two‐Step Chemoenzymatic Cascade for the Synthesis of a Bis‐benzofuran Derivative - Mertens - 2019 - European Journal of Organic Chemistry - Wiley Online Library
![Applied Sciences | Free Full-Text | Sequentially Palladium-Catalyzed Processes in One-Pot Syntheses of Heterocycles Applied Sciences | Free Full-Text | Sequentially Palladium-Catalyzed Processes in One-Pot Syntheses of Heterocycles](https://pub.mdpi-res.com/applsci/applsci-05-01803/article_deploy/html/images/applsci-05-01803-ag-550.jpg?1581038288)
Applied Sciences | Free Full-Text | Sequentially Palladium-Catalyzed Processes in One-Pot Syntheses of Heterocycles
![Development of a Water-Mediated and Catalyst-Free Green Protocol for Easy Access to a Huge Array of Diverse and Densely Functionalized Pyrido[2,3-d:6,5-d′]dipyrimidines via One-Pot Multicomponent Reaction under Ambient Conditions | ACS Sustainable ... Development of a Water-Mediated and Catalyst-Free Green Protocol for Easy Access to a Huge Array of Diverse and Densely Functionalized Pyrido[2,3-d:6,5-d′]dipyrimidines via One-Pot Multicomponent Reaction under Ambient Conditions | ACS Sustainable ...](https://pubs.acs.org/cms/10.1021/acssuschemeng.7b02696/asset/images/medium/sc-2017-02696k_0008.gif)
Development of a Water-Mediated and Catalyst-Free Green Protocol for Easy Access to a Huge Array of Diverse and Densely Functionalized Pyrido[2,3-d:6,5-d′]dipyrimidines via One-Pot Multicomponent Reaction under Ambient Conditions | ACS Sustainable ...
![An efficient one-pot four-component Gewald reaction: Synthesis of substituted 2-aminothiophenes with coumarin–thiazole scaffolds under environmentally benign conditions: Journal of Sulfur Chemistry: Vol 40, No 2 An efficient one-pot four-component Gewald reaction: Synthesis of substituted 2-aminothiophenes with coumarin–thiazole scaffolds under environmentally benign conditions: Journal of Sulfur Chemistry: Vol 40, No 2](https://www.tandfonline.com/cms/asset/24b3fc24-fd09-4bee-ab1f-00a5f5b20803/gsrp_a_1556275_uf0001_oc.jpg)