Literature DB >> 14507198

Iridium complex-catalyzed highly selective cross [2 + 2 + 2] cycloaddition of two different monoynes: 2:1 coupling versus 1:2 coupling.

Ryo Takeuchi1, Yoshihiko Nakaya.   

Abstract

[reaction: see text] Highly selective cross [2 + 2 + 2] cycloaddition of two different monoynes is achieved by using a catalytic amount of [Ir(cod)Cl](2) and ligand. The ligand had a considerable effect on the reaction. When 1,2-bis(diphenylphosphino)ethane was used, two molecules of dimethyl acetylenedicarboxylate (DMAD) reacted with one molecule of a monoyne to give the 2:1 coupling product. When 1,2-bis(dipentafluorophenylphosphino)ethane was used instead of dppe, one molecule of DMAD reacted with two molecules of a monoyne to give the 1:2 coupling product.

Entities:  

Year:  2003        PMID: 14507198     DOI: 10.1021/ol035330d

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


  4 in total

1.  Beyond Reppe: building substituted arenes by [2+2+2] cycloadditions of alkynes.

Authors:  Brandon R Galan; Tomislav Rovis
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

2.  Nickel-catalyzed cycloadditions of unsaturated hydrocarbons, aldehydes, and ketones.

Authors:  Thomas N Tekavec; Janis Louie
Journal:  J Org Chem       Date:  2008-03-05       Impact factor: 4.354

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.  Iridium-catalyzed intramolecular [4 + 2] cycloadditions of alkynyl halides.

Authors:  Andrew Tigchelaar; William Tam
Journal:  Beilstein J Org Chem       Date:  2012-10-16       Impact factor: 2.883

  4 in total

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