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SYNTHESIS OF REACTIVITY OF λ5-PHOSPHAZENES. USES AS SYNTHETIC INTERMEDIATES

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This article is published in Organic Preparations and Procedures International.The article was published on 1991-02-01. It has received 86 citations till now. The article focuses on the topics: Reactivity (chemistry).

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The aza-Wittig reaction: an efficient tool for the construction of carbon–nitrogen double bonds

TL;DR: Recent advances in the aza-Wittig reaction of phosphazene derivatives with several carbonyl compounds are reviewed in this article, where the most important applications of this reaction are the synthesis of a wide range of acyclic and heterocyclic compounds, ranging from simple moncyclic compounds to complex polycyclic and macrocyclic systems.
Journal ArticleDOI

Linear, cyclic and polymeric phosphazenes

TL;DR: An assessment of the diversity of phosphazene chemistry is presented in this paper with an emphasis on recent developments and their significance Fundamental properties of the phosphazenes are examined such as structure, nomenclature and bonding, and various synthetic procedures are catagorized.
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Alcohols for the α-Alkylation of Methyl Ketones and Indirect Aza-Wittig Reaction Promoted by Nickel Nanoparticles

TL;DR: Nickel nanoparticles have been found to activate primary alcohols used for the α-alkylation of ketones or in indirect aza-Wittig reactions as mentioned in this paper, and a reaction mechanism is proposed on the basis of some deuteration experiments.
References
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The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products

TL;DR: In this article, a reagent formed by combining diethyl azodicarboxylate (DEAD) and triphenylphosphine (TPP) could be utilized in the intermolecular dehydration between an alcohol and various acidic components such as carboxylic acids, phosphoric diesters, imides, and active methylene compounds.
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