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- W2783305684 endingPage "2103" @default.
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- W2783305684 abstract "Structurally diverse [5,n] bicyclic systems with cis ring junction stereochemistry were accessed readily through RRM (ring rearrangement metathesis) reaction of properly functionalized [2.2.1]norbornene skeletons. Several bicyclic enones, ketones, alcohols, and ethers acted as the substrates and yielded the respective linearly fused [5,n] bicyclic systems stereoselectively after the RRM reaction. Such [5,5]bicyclic enone scaffolds were then synthetically manipulated to core structural analogue of naturally occurring liner triquinane hirsutene having cis-syn-cis stereochemistry." @default.
- W2783305684 created "2018-01-26" @default.
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- W2783305684 date "2018-01-25" @default.
- W2783305684 modified "2023-10-16" @default.
- W2783305684 title "Exploration of Ring Rearrangement Metathesis Reaction: A General and Flexible Approach for the Rapid Construction [5,<i>n</i>]-Fused Bicyclic Systems en Route to Linear Triquinanes" @default.
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- W2783305684 doi "https://doi.org/10.1021/acs.joc.7b03021" @default.
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