Literature DB >> 22166119

A ridge walk between reaction modes: an unprecedented Pd-catalyzed domino sequence of diynyl-substituted bromoarenes.

Markus Leibeling1, Martin Pawliczek, Daniel Kratzert, Dietmar Stalke, Daniel B Werz.   

Abstract

Diynyl-substituted bromoarenes underwent a novel Pd-catalyzed domino reaction to provide benzofurans, pyridinofurans, isochromenes, and indole derivatives. Slight changes of the substrate push the reaction in another direction resulting in benzene annulation.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID： 22166119     DOI： 10.1021/ol2030923

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  3 in total

1.  Flexible synthesis of anthracycline aglycone mimics via domino carbopalladation reactions.

Authors:  Markus Leibeling; Daniel B Werz
Journal:  Beilstein J Org Chem       Date:  2013-10-24       Impact factor: 2.883

2.  Palladium-catalyzed Tsuji-Trost-type reaction of benzofuran-2-ylmethyl acetates with nucleophiles.

Authors:  Antonio Arcadi; Giancarlo Fabrizi; Andrea Fochetti; Francesca Ghirga; Antonella Goggiamani; Antonia Iazzetti; Federico Marrone; Giulia Mazzoccanti; Andrea Serraiocco
Journal:  RSC Adv       Date:  2021-01-04       Impact factor: 3.361

3.  Total Synthesis of Cyclopiamide A Using Palladium-Catalyzed Domino Cyclization.

Authors:  Sunhwa Park; Kye Jung Shin; Jae Hong Seo
Journal:  Molecules       Date:  2020-10-23       Impact factor: 4.411
  3 in total

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