Publication | Closed Access
The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
4.1K
Citations
15
References
1981
Year
EngineeringDiethyl AzodicarboxylateBiochemistryNatural SciencesActive Methylene CompoundsOrganic ChemistryNatural ProductsStereoselective SynthesisChemistryPharmacologyCyclic EthersDerivative (Chemistry)Synthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringNatural Product Synthesis
Abstract The 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. By the use of DEAD and TPP, diols and hydroxy acids gave cyclic ethers and lactones, respectively. The reaction of nucleosides with DEAD and TPP afforded triphenylphosphoranylnucleosides. Alcohols reacted with 2,6-di-t-butyl-4-nitrophenol in the presence of DEAD and TPP to give aci-nitroesters which converted into the corresponding carbonyl compounds.
| Year | Citations | |
|---|---|---|
Page 1
Page 1