Repository landing page
Base-Promoted Synthesis of <i>N</i>‑Substituted 1,2,3-Triazoles via Enaminone–Azide Cycloaddition Involving Regitz Diazo Transfer
Abstract
The domino reactions between NH-based secondary enaminones and tosyl azide have been developed for the synthesis of various <i>N</i>-substituted 1,2,3-triazoles by employing <i>t</i>-BuONa as the base promoter. Through a key Regitz diazo-transfer process with tosyl azide, the reactions proceed efficiently at room temperature with good substrate tolerance- Dataset
- Dataset
- Biophysics
- Biochemistry
- Microbiology
- Genetics
- Biotechnology
- Evolutionary Biology
- Ecology
- Mental Health
- Infectious Diseases
- Plant Biology
- Computational Biology
- Environmental Sciences not elsewhere classified
- Biological Sciences not elsewhere classified
- Chemical Sciences not elsewhere classified
- Information Systems not elsewhere classified
- domino
- Enaminone
- NH-based
- Triazole
- triazole
- Substituted
- enaminone
- Synthesi
- BuONa
- Base-Promoted
- Regitz diazo-transfer process
- substrate
- tolerance
- promoter
- tosyl azide
- synthesis
- Cycloaddition
- Regitz Diazo Transfer
Similar works
Full text
Last time updated on 12/02/2018
This paper was published in The Francis Crick Institute.
Having an issue?
Is data on this page outdated, violates copyrights or anything else? Report the problem now and we will take corresponding actions after reviewing your request.