Synthesis Of Onychine By Cycloaddition/Cycloreversion Of An Intermediate 1,2,4-Triazine
2024
- 24Usage
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Usage24
- Abstract Views23
- Downloads1
Thesis / Dissertation Description
This study investigates the synthetic sequence for the preparation of onychine, a natural product with antifungal activity. The scaffold is accessed through an azafluorenone intermediate prepared by a Diels-Alder/retro-Diels-Alder cycloaddition/cycloreversion of a ninhydrin-derived 1,2,4-triazine precursor. Downstream elaboration towards the alkaloid core structure is made through complementary condensation and aromatic nucleophilic substitution (SNAr) strategies.
Bibliographic Details
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