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Reactions of O-silylated enolates with allylsilane bifunctional [4+2] and [5+2] annulating reagents

✍ Scribed by Thomas V. Lee; Raymond J. Boucher; John R. Porter; Caroline J.M. Rockell


Publisher
Elsevier Science
Year
1989
Tongue
French
Weight
433 KB
Volume
45
Category
Article
ISSN
0040-4020

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✦ Synopsis


Stunmary: The reactions of the two aliylsilane-acetals (8) and (9) with various 0-silylated enolates is described. This has resulted in a new route to fused carbocyclic six and seven-membered rings in a one-pot reaction by use of a chemospecific allylsilane based bijknctional annulating reagent.


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Gold-Catalyzed 5- and 6-exo-dig Selectiv
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## Abstract An efficient method for the annulation of five‐ and six‐membered rings onto Ξ±,β‐enones is described __via__ gold‐catalyzed 5‐ and 6‐__exo__‐__dig__ selective cyclizations of alkynyl silyl enol ethers.