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Reduction of the 2‐azetidinone moiety in the polymer main chain: A novel synthetic route to polyamine with hydroxymethyl pendant
Authors:Atsushi Sudo  Masato Sato  Takeshi Endo
Abstract:A polymer with a 2‐azetidinone moiety in its main chain was efficiently synthesized by 2 + 2] cycloaddition of bisimine with bisketene. The bisketene was easily prepared by dehydrochlorination of the corresponding dicarboxylic acid chloride and was used without purification. The treatment of the obtained polymer with lithium aluminum hydride resulted in a reductive ring‐opening reaction of the 2‐azetidinone moiety in the main chain that gave the corresponding linear polyamine with hydroxymethyl side chains. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3789–3796, 2001
Keywords:2‐azetidinone  [2 + 2] cycloaddition  bisketene  reduction  lithium aluminum hydride  ring opening  differential scanning calorimetry (DSC)  polyamines  thermal properties
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