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Synthesis of ent-[3]-Ladderanol: Development and Application of Intramolecular Chirality Transfer [2+2] Cycloadditions of Allenic Ketones and Alkenes

An enantioselective synthesis of ent-[3]-ladderanol is presented. The ladderanes are an interesting class of molecules for their unique structure of fused cyclobutane rings as well as their perceived biological function of organism protection. The route hinges on the development and application of a...

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Published in:Journal of the American Chemical Society 2017-10, Vol.139 (41), p.14392-14395
Main Authors: Line, Nathan J, Witherspoon, Brittany P, Hancock, Erin N, Brown, M. Kevin
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Language:English
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cited_by cdi_FETCH-LOGICAL-a516t-9269258ee0234dd55e6de14269f46163ac43dfb09cdf831804df959b420c06f23
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creator Line, Nathan J
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description An enantioselective synthesis of ent-[3]-ladderanol is presented. The ladderanes are an interesting class of molecules for their unique structure of fused cyclobutane rings as well as their perceived biological function of organism protection. The route hinges on the development and application of a chirality transfer [2+2] cycloaddition of an allenic ketone and alkene. Further stereocontrolled transformations allowed for completion of the synthesis. The scope of the chirality transfer [2+2] cycloaddition is also presented.
doi_str_mv 10.1021/jacs.7b09844
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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects alkenes
Alkenes - chemistry
Cycloaddition Reaction
cycloaddition reactions
Cyclobutanes - chemistry
enantioselective synthesis
ketones
Ketones - chemistry
optical isomerism
Stereoisomerism
title Synthesis of ent-[3]-Ladderanol: Development and Application of Intramolecular Chirality Transfer [2+2] Cycloadditions of Allenic Ketones and Alkenes
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