Progress Toward the Total Synthesis of Bielschowskysin: A Stereoselective [2+2] Photocycloaddition

The tetracyclic core of the diterpene bielschowskysin has been prepared as a single enantiomer via a stereoselective intramolecular [2 + 2] photocycloaddition of 5-alkylidene-2(5H)-furanone 3.

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PID pmc:PMC2527052
PID https://www.doi.org/10.1021/ol0530225
PID pmid:16494470
PID https://www.doi.org/10.1021/ol0530225.s001
PID https://www.doi.org/10.1021/ol0530225.s002
URL https://europepmc.org/articles/PMC2527052/
URL https://figshare.com/articles/journal_contribution/Progress_toward_the_Total_Synthesis_of_Bielschowskysin_A_Stereoselective_2_2_Photocycloaddition/3235441
URL http://dx.doi.org/10.1021/ol0530225
URL http://europepmc.org/articles/pmc2527052?pdf=render
URL https://figshare.com/articles/journal_contribution/Progress_toward_the_Total_Synthesis_of_Bielschowskysin_A_Stereoselective_2_2_Photocycloaddition/3235450
URL https://pubs.acs.org/doi/pdf/10.1021/ol0530225
URL https://academic.microsoft.com/#/detail/2015435203
URL https://pubs.acs.org/doi/abs/10.1021/ol0530225
URL https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527052/
URL http://europepmc.org/abstract/MED/16494470
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Access Right Open Access
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Author Doroh, Brandon
Author Sulikowski, Gary A.
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Collected From PubMed Central; UnpayWall; Datacite; figshare; Crossref; Microsoft Academic Graph
Hosted By Europe PubMed Central; Organic Letters; figshare
Publication Date 2016-05-05
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Language English
Resource Type Other literature type; Article
system:type publication
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Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::5238dcb97d2ca281fc9480029a1d850b
Author jsonws_user
Last Updated 22 December 2020, 23:16 (CET)
Created 22 December 2020, 23:16 (CET)