Anodic oxidation of 4-methoxy-1-naphthol

doi:10.1016/S0040-4039(02)00544-0

Paper

Anodic oxidation of 4-methoxy-1-naphthol

Published Apr 29, 2002 · H. El-Seedi, S. Yamamura, S. Nishiyama

Tetrahedron Letters

Q3 SJR score

12

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0

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Abstract

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Study Snapshot

Anodic oxidation of 4-methoxy-1-naphthol produces products 8-12 and dimers 13 and 17, with the reaction mechanism including [3+2] cycloaddition.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Paper

Anodic oxidation of 4-methoxy-1-naphthol

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References

Total synthesis of the gilvocarcins

The synthesis of gilvocarcin M and V provides a new strategy for the development of new antibiotics against various bacterial infections.

A facile synthesis of naturally occurring binaphthoquinones: efficient oxidative dimerization of 4-alkoxy-1-naphthols using silver(II) oxide–40% nitric acid

Silver(II) oxide-nitric acid-based oxidative dimerization efficiently synthesizes naturally occurring binaphthoquinones, bivitamin K3 and 3,3′-bijuglone.

Studies in natural products chemistry

Advances in spectroscopic techniques and high-throughput screening techniques have made it possible to rapidly isolate and determine the structures and biological activity of natural products, offering exciting opportunities for new drug development in the pharmaceutical industry.

Citations

Electrochemical strategies for C-H functionalization and C-N bond formation.

Electrochemical synthesis offers a sustainable, scalable strategy for achieving challenging carbon-carbon and carbon-heteroatom bonds, offering environmentally benign, effective, and versatile solutions for future synthetic applications.

Betaine mediated synthesis of annulated dihydrofurans from oxobis(methylthio)ketene acetals and N-butyl-N'-methyl ethane-1,2-diamine as precursors via NHC elimination.

This study developed a new method for synthesis of annulated dihydrofurans using oxobis(methylthio)ketene acetals and N-butyl-N'-methyl ethane-1,2-diamine, enabling selective C-C and C-O bond formation

Photocatalytic synthesis of dihydrobenzofurans by oxidative [3+2] cycloaddition of phenols.

This study presents a photocatalytic method for the modular synthesis of dihydrobenzofurans using ammonium persulfate as a benign terminal oxidant, offering potential for various useful oxidative transformations.

Anodic fluorination of 4-methoxy-1-naphthol and 4-nitroanisole using Et3N · 5 HF in mixed nonaqueous solvent

Anodic fluorination of 4-methoxy-1-naphthol and 4-nitroanisole in mixed nonaqueous solvent using Et3N 5 HF provides excellent yield, short reaction time, and easy work-up, offering advantages in green chemistry.

Appendix N

This appendix contains citations accepted by ECOTOX for carbaryl and degradates of carbaryl, as well as papers meeting the minimum criteria for inclusion in the database.