[3 + 2] Cycloaddition of acetylenes with azides to give 1,4-disubstituted 1,2,3-triazoles in a modular flow reactor
The cycloaddition of acetylenes with azides to give the corresponding 1,4-disubstituted 1,2,3-triazoles is reported using immobilised reagents and scavengers in pre-packed glass tubes in a modular flow reactor.
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| Veröffentlicht in: | Organic & biomolecular chemistry 2007-05, Vol.5 (10), p.1559-1561 |
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| container_end_page | 1561 |
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| container_issue | 10 |
| container_start_page | 1559 |
| container_title | Organic & biomolecular chemistry |
| container_volume | 5 |
| creator | Smith, Christopher D Baxendale, Ian R Lanners, Steve Hayward, John J Smith, Stephen C Ley, Steven V |
| description | The cycloaddition of acetylenes with azides to give the corresponding 1,4-disubstituted 1,2,3-triazoles is reported using immobilised reagents and scavengers in pre-packed glass tubes in a modular flow reactor. |
| doi_str_mv | 10.1039/b702995k |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1477-0520 |
| ispartof | Organic & biomolecular chemistry, 2007-05, Vol.5 (10), p.1559-1561 |
| issn | 1477-0520 1477-0539 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_70619528 |
| source | MEDLINE; Royal Society of Chemistry Journals Archive (1841-2007); Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| subjects | Alkynes - chemistry Azides - chemistry Catalysis Chemistry, Pharmaceutical - instrumentation Chemistry, Pharmaceutical - methods Copper - chemistry Equipment Design Magnetic Resonance Spectroscopy Models, Chemical Peptides - chemistry Triazoles - chemistry |
| title | [3 + 2] Cycloaddition of acetylenes with azides to give 1,4-disubstituted 1,2,3-triazoles in a modular flow reactor |
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