Reaction of Derivatives of the [2+2]-Cycloadduct of Dichloroketene and Dimethylfulvene with Ozone
Russian Journal of Organic Chemistry, ISSN: 1608-3393, Vol: 60, Issue: 2, Page: 349-352
2024
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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.
Article Description
Abstract: Previously unknown optically active cyclopentenones were synthesized by the ozonation of 2-dichloromethyl-5-(1-methylethylidene)-N-[(1R)-1-phenylethyl]cyclopent-3-ene-1-carboxamide in CHCl–MeOH (10 : 1) at 0°C and of (3aR,6aR)-3-hydroxy-6-(1-methylethylidene)-2-[(1R)-1-phenylethyl)-3,3a,6,6a-tetrahydrocyclopenta[c]pyrrol-1(2H)-one in cyclohexane–MeOH (10 : 1) at 5°C until complete consumption of the starting compounds (by TLC), followed by treatment with MeS. The new obtained cyclopentenons: 2-(dichloromethyl)-5-oxo-N-[(1R)-1-phenylethyl]cyclopent-3-ene-1-carboxamide and (3aR,6aR)-3-hydroxy-2-[(1R)-1-phenylethyl]-2,3,3a,6a-tetrahydrocyclopenta[c]pyrrole-1,6-dione are useful compounds to prepare cyclopentanoids.
Bibliographic Details
Pleiades Publishing Ltd
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