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Synthesis of fluorenyl alcohols via cooperative palladium/norbornene catalysis
Herein, we report a novel catalytic synthesis of substituted 9H-fluoren-9-ols starting from aryl iodides and secondary ortho-bromobenzyl alcohols in the presence of palladium/norbornene as a catalytic system. The present protocol exhibits high functional group tolerance, mild reaction conditions and...
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Published in: | Organic & biomolecular chemistry 2019-06, Vol.17 (25), p.6165-6173 |
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container_title | Organic & biomolecular chemistry |
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creator | Casnati, Alessandra Fontana, Marco Motti, Elena Della Ca', Nicola |
description | Herein, we report a novel catalytic synthesis of substituted 9H-fluoren-9-ols starting from aryl iodides and secondary ortho-bromobenzyl alcohols in the presence of palladium/norbornene as a catalytic system. The present protocol exhibits high functional group tolerance, mild reaction conditions and moderate to good yields. This transformation is based on two sequential pathways: (i) Pd(ii)-mediated oxidation of the secondary alcohol to the corresponding ketone and (ii) Pd(0)/norbornene-catalyzed reaction of the in situ generated ortho-bromoacetophenone with the aryl iodide. |
doi_str_mv | 10.1039/c9ob01085h |
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subjects | Alcohol Alcohols Aromatic compounds Catalysis Chemical synthesis Functional groups Iodides Oxidation Palladium |
title | Synthesis of fluorenyl alcohols via cooperative palladium/norbornene catalysis |
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