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Synthesis of substituted allyl acetates from heterocyclic dienes by a Pd-promoted arylation-acetoxylation cascade

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2017
2840.pdf (962.6Kb)
Authors
Simić, Milena
Petković, Miloš
Jovanović, Predrag
Tasić, Gordana
Savić, Vladimir
Article (Published version)
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Abstract
Pd-catalysed arylation-acetoxylation cascade, a previously reported methodology, was applied in the functionalisation of unsymmetrical dienes. Both explored classes of compounds, isoquinoline and ss-carboline-derived dienes, afforded single regioisomers. Although further improvements of the process are necessary, primarily due to lower yields, the described functionalisation of the studied compounds might be useful in the synthesis of emetine and related naturally occurring compounds.
Source:
Journal of the Serbian Chemical Society, 2017, 82, 12, 1335-1341
Publisher:
  • Srpsko hemijsko društvo, Beograd
Projects:
  • Computational design, synthesis and biological evaluation of new heterocyclic compounds as selective tumorogenesis inhibitors (RS-172009)

DOI: 10.2298/JSC170317046S

ISSN: 0352-5139

WoS: 000419391700001

Scopus: 2-s2.0-85040055713
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URI
http://farfar.pharmacy.bg.ac.rs/handle/123456789/2842
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  • Radovi istraživača / Researchers’ publications
Institution
Pharmacy

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