Literature DB >> 18052296

Microwave-mediated nickel-catalyzed cyclotrimerization reactions: total synthesis of illudinine.

Jesse A Teske1, Alexander Deiters.   

Abstract

Rapid and efficient [2 + 2 + 2] cyclotrimerization reactions were discovered through the application of microwave irradiation in conjunction with a Ni(CO)(2)(PPh(3))(2) catalyst. This enables the facile construction of highly substituted indane, isoindoline, and tetraline core structures. The developed microwave-mediated Ni-catalyzed cyclotrimerization reaction was employed as the key step in a concise synthesis of the isoquinoline natural product illudinine. This represents the first example of a Ni-catalyzed cyclotrimerization reaction in total synthesis.

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Year:  2007        PMID: 18052296     DOI: 10.1021/jo7020955

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  4 in total

Review 1.  Controlled microwave heating in modern organic synthesis: highlights from the 2004-2008 literature.

Authors:  C Oliver Kappe; Doris Dallinger
Journal:  Mol Divers       Date:  2009-04-21       Impact factor: 2.943

2.  Multicomponent reaction access to complex quinolines via oxidation of the Povarov adducts.

Authors:  Esther Vicente-García; Rosario Ramón; Sara Preciado; Rodolfo Lavilla
Journal:  Beilstein J Org Chem       Date:  2011-07-13       Impact factor: 2.883

3.  Enhanced Catalytic Activity of Nickel Complexes of an Adaptive Diphosphine-Benzophenone Ligand in Alkyne Cyclotrimerization.

Authors:  Alessio F Orsino; Manuel Gutiérrez Del Campo; Martin Lutz; Marc-Etienne Moret
Journal:  ACS Catal       Date:  2019-01-31       Impact factor: 13.084

4.  Air-Stable CpCoI-Phosphite-Fumarate Precatalyst in Cyclization Reactions: Comparing Different Methods of Energy Supply.

Authors:  Fabian Fischer; Marko Hapke
Journal:  European J Org Chem       Date:  2018-06-21
  4 in total

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