Carbon-carbon bond forming reactions of rhenium enolates with terminal alkynes. Evidence for an alkyne C-H oxidative addition mechanism and observation of highly stereoselective base-catalyzed proton transfer reactions in rhenium metallacycles
摘要:
The acetonitrile-substituted complex (I), its CH(Me)-COOEt analogue, and the chelating amide complex (V) react with terminal alkynes as demonstrated for the example (I) with (II) to afford less thermodynamically stable five-membered metallacycles with Z stereochemistry of the type (III).
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DOI:
10.1002/chin.199030251
被引量:
年份:
1990
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