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À propos de : Protected Indanones by a Heck−AldolAnnulation Reaction        

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  • Protected Indanones by a Heck−AldolAnnulation Reaction
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  • Monoprotected 3-hydroxyindan-1-ones have beenprepared in moderate to good yields by a new tandemreaction involving salicylaldehyde triflates and commerciallyavailable 2-hydroxyethyl vinyl ether. This one-pot annulation reaction proceeds in the presence of a palladiumbidentate catalyst and results in the formation of two newring systems.
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