866006-63-5Relevant academic research and scientific papers
A benzannulation strategy for the synthesis of phenols and heteroaromatic compounds based on the reaction of (trialkylsilyl)vinylketenes with lithium ynolates
Austin, Wesley F.,Zhang, Yongjun,Danheiser, Rick L.
, p. 915 - 925 (2008/09/16)
(Trialkylsilyl)vinylketenes react with lithium ynolates to generate 3-(oxido)dienylketenes, which undergo rapid 6π-electrocyclization. The ultimate products of this benzannulation are highly substituted resorcinol monosilyl ethers, which are formed via a [1,3] carbon to oxygen silyl?group shift. Further transformations of the benzannulation products are described providing efficient access to ortho-benzoquinones and benzofuran, benzoxepine, and benzoxocine ring systems.
Reactions of (Trialkylsilyl)vinylketenes with lithium ynolates: A new benzannulation strategy
Austin, Wesley F.,Zhang, Yongjun,Danheiser, Rick L.
, p. 3905 - 3908 (2007/10/03)
(Chemical Equation Presented) (Trialkylsilyl)vinylketenes react with lithium ynolates to produce highly substituted phenols in a new benzannulation strategy that proceeds via the 6π electrocyclization of an intermediate 3-(oxido)dienylketene.
