Return to search

Trimethylsilylbromoketene and reactions of α-haloacid halides with diisopropylcarbodiimide

Trimethylsilylbromoketene was synthesized by the tri-ethylamine dehydrohalogenation of trimthylsilylbromacetyl bromide or chloride. This ketene was found not to undergo cycloaddition reactions with activated olefins, such as cyclopentadiene, ethyl vinyl ether and dihydropyan.

Identiferoai:union.ndltd.org:unt.edu/info:ark/67531/metadc332482
Date05 1900
CreatorsOwens, Robert Austin
PublisherNorth Texas State University
Source SetsUniversity of North Texas
LanguageEnglish
Detected LanguageEnglish
TypeThesis or Dissertation
FormatText
RightsPublic, Owens, Robert Austin, Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved.

Page generated in 0.0017 seconds