<i>N</i>-Halosuccinimides as Precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction Conditions
<i>N</i>-halosuccinimides (chloro, bromo, and iodo, respectively) were introduced, tested, and applied as efficient and non-metal precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-nucleophilic substitution reactions of alcohols...
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| Format: | Article |
| Language: | English |
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MDPI AG
2020-04-01
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| Series: | Catalysts |
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| Online Access: | https://www.mdpi.com/2073-4344/10/4/460 |
| _version_ | 1797569730508226560 |
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| author | Njomza Ajvazi Stojan Stavber |
| author_facet | Njomza Ajvazi Stojan Stavber |
| author_sort | Njomza Ajvazi |
| collection | DOAJ |
| description | <i>N</i>-halosuccinimides (chloro, bromo, and iodo, respectively) were introduced, tested, and applied as efficient and non-metal precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-nucleophilic substitution reactions of alcohols under solvent-free reaction conditions (SFRC) or under high substrate concentration reaction conditions (HCRC) efficiently and selectively, into the corresponding products. |
| first_indexed | 2024-03-10T20:15:41Z |
| format | Article |
| id | doaj.art-a5587c4eb22f4321990ce0e7992a1326 |
| institution | Directory Open Access Journal |
| issn | 2073-4344 |
| language | English |
| last_indexed | 2024-03-10T20:15:41Z |
| publishDate | 2020-04-01 |
| publisher | MDPI AG |
| record_format | Article |
| series | Catalysts |
| spelling | doaj.art-a5587c4eb22f4321990ce0e7992a13262023-11-19T22:36:30ZengMDPI AGCatalysts2073-43442020-04-0110446010.3390/catal10040460<i>N</i>-Halosuccinimides as Precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction ConditionsNjomza Ajvazi0Stojan Stavber1Jožef Stefan International Postgraduate School, Jamova 39, 1000 Ljubljana, SloveniaJožef Stefan International Postgraduate School, Jamova 39, 1000 Ljubljana, Slovenia<i>N</i>-halosuccinimides (chloro, bromo, and iodo, respectively) were introduced, tested, and applied as efficient and non-metal precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-nucleophilic substitution reactions of alcohols under solvent-free reaction conditions (SFRC) or under high substrate concentration reaction conditions (HCRC) efficiently and selectively, into the corresponding products.https://www.mdpi.com/2073-4344/10/4/460alcohols<i>N</i>-halosuccinimidesC–C or C–heteroatom bond formationsolvent-freegreen chemistry |
| spellingShingle | Njomza Ajvazi Stojan Stavber <i>N</i>-Halosuccinimides as Precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction Conditions Catalysts alcohols <i>N</i>-halosuccinimides C–C or C–heteroatom bond formation solvent-free green chemistry |
| title | <i>N</i>-Halosuccinimides as Precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction Conditions |
| title_full | <i>N</i>-Halosuccinimides as Precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction Conditions |
| title_fullStr | <i>N</i>-Halosuccinimides as Precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction Conditions |
| title_full_unstemmed | <i>N</i>-Halosuccinimides as Precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction Conditions |
| title_short | <i>N</i>-Halosuccinimides as Precatalysts for <i>C</i>-, <i>N</i>-, <i>O</i>-, and <i>X</i>-Nucleophilic Substitution Reactions of Alcohols under Mild Reaction Conditions |
| title_sort | i n i halosuccinimides as precatalysts for i c i i n i i o i and i x i nucleophilic substitution reactions of alcohols under mild reaction conditions |
| topic | alcohols <i>N</i>-halosuccinimides C–C or C–heteroatom bond formation solvent-free green chemistry |
| url | https://www.mdpi.com/2073-4344/10/4/460 |
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