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- W2343973669 endingPage "9129" @default.
- W2343973669 startingPage "9125" @default.
- W2343973669 abstract "An unprecedented access to strained tetracyclic bridgehead alkenes by reaction of easily accessible ortho-alkynylarylaldehydes with conjugated dienes is described. The process involves a chemo- and stereo-selective, gold-catalyzed, tandem intermolecular [3+2] cycloaddition/Prins-type ring-closing reaction that allows generating structural complexity in a straightforward manner. This approach for the preparation of anti-Bredt compounds is synthetically superior to those previously reported: the procedure is easy to implement, operates under mild experimental conditions, is efficient, and exhibits a good substrate scope." @default.
- W2343973669 created "2016-06-24" @default.
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- W2343973669 creator A5069147938 @default.
- W2343973669 date "2016-05-24" @default.
- W2343973669 modified "2023-10-18" @default.
- W2343973669 title "Gold-Catalyzed Reaction of<i>ortho</i>-Alkynylarylaldehydes with Conjugated Dienes: An Efficient Access to Highly Strained Tetracyclic Bridgehead Olefins" @default.
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