ChemInform Abstract: PREPARATION AND REACTIONS OF 1,3‐BIS(TRIMETHYLSILYLOXY)ISOBENZOFURANS AND ‐ISOINDOLES

Troll, T.; Ollmann, Georg W.

doi:10.1002/chin.198201203

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2013

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“…Isoindoles are promising active biological materials [1,2] with interesting spectral properties and are the subject of studies for important theoretical questions, such as: aromaticity, tautomerism [3][4][5][6][7] and represent an important source of reagents used in cycloaddition reactions, [8][9][10][11][12] the study of organic reaction mechanisms, new rearrangements [13,14].…”

Section: Introductionmentioning

confidence: 99%

Synthesis, Autoorganization and Reactivity of Amphiphilic Derivatives of 1‐Aminoisoindole in Water and Formamide

Levkov

Cassel

Voitenko

et al. 2013

J Surfact & Detergents

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In this work, we present the synthesis of cationic surfactants based on 1-aminoisoindole. The physico-chemical properties were studied by conductometry, tensiometry, dynamic light scattering and transmission electron microscopy in water and in formamide. The reactivity of these novel surfactants has been studied at concentrations below and above critical aggregation concentrations (CAC) and it was found that reactions can proceed in structured media without the addition of other catalysts.

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Section: Introductionmentioning

confidence: 99%

Synthesis, Autoorganization and Reactivity of Amphiphilic Derivatives of 1‐Aminoisoindole in Water and Formamide

Levkov

Cassel

Voitenko

et al. 2013

J Surfact & Detergents

View full text Add to dashboard Cite

show abstract

ChemInform Abstract: PREPARATION AND REACTIONS OF 1,3‐BIS(TRIMETHYLSILYLOXY)ISOBENZOFURANS AND ‐ISOINDOLES

Abstract: Bei der elektrolytischen Reduktion der Phthalsäureanhydride (Ia)‐(Id) bzw. (IV) in Gegenwart von Trimethylchlorsilan (II) entstehen die Diphthalylsäurelactonether (III) bzw. (V); aus (IV) erhält man zusätzlich ein polycyclisches Dimerisierungsprodukt (VI).

Cited by 1 publication

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Synthesis, Autoorganization and Reactivity of Amphiphilic Derivatives of 1‐Aminoisoindole in Water and Formamide

Synthesis, Autoorganization and Reactivity of Amphiphilic Derivatives of 1‐Aminoisoindole in Water and Formamide

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