The high yield and regioselective conversion of an unactivated aziridine to an oxazolidinone using carbon dioxide with ammonium iodide as the catalyst-Reference-Cited by-同舟云学术

The high yield and regioselective conversion of an unactivated aziridine to an oxazolidinone using carbon dioxide with ammonium iodide as the catalyst

Published:2010-08 Issue:34 Volume:51 Page:4552-4554
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Phung Chau,Pinhas Allan R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. Oxazolidin-2-one Ring, a Popular Framework in Synthetic Organic Chemistry: Part 1. The Construction of the Oxazolidin-2-one Ring

2. Advances in Nitrogen Transfer Reactions Involving Aziridines

3. Nucleophilic ring opening of aziridines

4. Transformation of Carbon Dioxide

5. Catalysis Research of Relevance to Carbon Management: Progress, Challenges, and Opportunities

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2. Application of CO2 as С1-Synthon in Organic Chemistry: II: Catalytic Synthesis of Cyclic Carbonates (Carbamates) from CO2 and Epoxides (Aziridines);Журнал органической химии;2023-08-15

3. Application of CO2 as a C1-Synthon in Organic Chemistry: II. Catalytic Synthesis of Cyclic Carbonates (Carbamates) from CO2 and Epoxides (Aziridines);Russian Journal of Organic Chemistry;2023-08

4. B−N Coordinated Phenanthroimidazole‐Based Zinc‐Salen as a Photocatalyst for the Synthesis of Oxazolidinones using Carbon Dioxide as a C1 Source under Mild Reaction Conditions;Advanced Synthesis & Catalysis;2023-01-13

5. Recent advances on oxazolidinones synthesize from carbon dioxide;Journal of Fuel Chemistry and Technology;2023-01