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Staudinger’s phosphazene as an efficient esterifying reagent
Version 2 2016-08-26, 21:42
Version 1 2016-07-18, 16:25
journal contribution
posted on 2016-08-26, 21:42 authored by Murugan Dinesh, Raja Ranganathan, Sivasubramaniyan Archana, Murugan Sathishkumar, Mohamed Sulthan Roshan Banu, Alagusundaram PonnuswamyA new application of Staudinger’s phosphazene as an efficient esterifying reagent is reported. Staudinger’s phosphazene formed in situ by the reaction of organic mono-azide with triphenylphosphine, which is trapped by carboxylic acid, to afford amide exclusively. In contrast, interestingly the same phosphazene behaves in a different way as an efficient esterifying reagent, affording ester under a solvent-free microwave-assisted protocol wherein alcohol is added as the another component in addition to the other reactants. This discovery adds yet another new application of Staudinger’s phosphazene to synthetic chemistry.