Literature DB >> 17015975

A green method for the electroorganic synthesis of new 1,3-Indandione derivatives.

Abdolmajid Bayandori Moghaddam1, Mohammad Reza Ganjali, Parviz Norouzi, Maryam Latifi.   

Abstract

This is an environmentally friendly method in the field of electroorganic reactions under controlled potential electrolysis, without toxic reagents at a carbon electrode in an undivided cell which involves the (EC) mechanism reaction and comprises two steps alternatively; (i) electrochemical oxidation and (ii) chemical reaction. In particular, the electrochemical oxidation of 4-tert-butylcatechol, 4-methylcatechol and 2,3-dihydroxybenzoic acid in the presence of 2-phenyl-1,3-indandione has been studied in a water-acetonitrile (90 : 10) mixture. The research includes the use of a variety of experimental techniques, such as cyclic voltammetry, controlled-potential electrolysis, and spectroscopic identification of products (FT-IR, (1)H-NMR, and MS spectrometry).

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Year:  2006        PMID: 17015975     DOI: 10.1248/cpb.54.1391

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  2 in total

1.  Molecular geometry, vibrations and electrode potentials of 2-(4,5-dihydroxy-2-methylphenyl)-2-phenyl-2H-indene-1,3-dione; experimental and theoretical attempts.

Authors:  Siavash Riahi; Mohammad Reza Ganjali; Abdolmajid Bayandori Moghaddam; Parviz Norouzi
Journal:  J Mol Model       Date:  2008-02-15       Impact factor: 1.810

2.  Electrochemical synthesis of novel 1,3-indandione derivatives and evaluation of their antiplatelet aggregation activities.

Authors:  Salimeh Amidi; Farzad Kobarfard; Abdolmajid Bayandori Moghaddam; Kimia Tabib; Zohreh Soleymani
Journal:  Iran J Pharm Res       Date:  2013       Impact factor: 1.696

  2 in total

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