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Pd(0)-catalyzed alkenylation and allylic dearomatization reactions between nucleophile-bearing indoles and propargyl carbonate. | LitMetric

Pd(0)-catalyzed alkenylation and allylic dearomatization reactions between nucleophile-bearing indoles and propargyl carbonate.

Org Lett

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , 345 Lingling Lu, Shanghai 200032, China.

Published: August 2014

AI Article Synopsis

  • Spiroindolenine derivatives are created using a reaction that involves a palladium catalyst and indoles.
  • This process involves the interaction of indoles with propargyl carbonate in a step-by-step manner.
  • The method results in the formation of spiroindolenines or spiroindolines with high efficiency, yielding good to excellent amounts of product.

Article Abstract

Spiroindolenine derivatives were synthesized by intermolecular Pd-catalyzed dearomatization of indoles. The reaction between nucleophile bearing indoles and propargyl carbonate proceeds in a cascade fashion providing spiroindolenines or spiroindolines in good to excellent yields.

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Source
http://dx.doi.org/10.1021/ol501704qDOI Listing

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