catalytic
The abstract lacks a clear statement of conclusions or broader implications. Adding one sentence about the significance would strengthen the abstract in terms of future applications.
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pubs.acs.org pubs.acs.org
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similar
The abstract presents a clear progression from methods to results, making it easy for readers to understand the synthetic transformation being reported. The inclusion of both regioselectivity and mechanistic information (SN2-type) provides depth that helps readers assess the methods.
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conditions
This abstract lacks an explicit conclusions section. The abstract presents results, but doesn't explicitly state what these results mean for future applications.
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In most cases, this ring-opening transformation proceeds with highregioselectivity, favoring nucleophilic attack at the more substituted position of theepoxide
This presents the experimental observation that the reaction shows regioselective preference for attack at the more substituted epoxide carbon.
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Upon treatment with a catalytic amount of BF3·OEt2
This identifies the key approach, specifying that BF₃OEt₂ is used as a catalyst to facilitate the ring-opening reaction.
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he reactionbetween azulene derivatives and epoxides efficiently affords azulenylethanolderivatives
This section establishes the main objective of the research: to demonstrate a synthetic route for producing azulenylethananol derivatives through a reaction between azulene derivatives and epoxides.
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