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https://doi.org/10.1002/slct.201802090
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Cite Journal: ChemistrySelect |  Publication Date: Nov 21, 2018 |
 Citations: 1 |
Affiliation: University of Wollongong
AbstractA highly stereoselective and an efficient approach for studies towards the synthesis of Cruentaren B has been described. The key steps involved in this synthesis are Prins cyclisation, nucleophilic epoxide ring opening, Alder‐Rickert reaction, SN2 displacement reaction and Lindlar's hydrogenation.
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