Literature DB >> 18217604

Facile formation of iodocyclobutenes by a ruthenium-catalyzed enyne cycloisomerization.

Alois Fürstner1, Andreas Schlecker, Christian W Lehmann.   

Abstract

Enynes bearing an iodide (bromide) at their alkyne terminus react with catalytic amounts of [Cp*Ru(MeCN)3]PF6 in DMF to give strained iodo(bromo)cyclobutene derivatives in good to excellent yields.

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Year:  2007        PMID: 18217604     DOI: 10.1039/b708903a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Differential reactivities of enyne substrates in ruthenium- and palladium-catalyzed cycloisomerizations.

Authors:  Barry M Trost; Alicia C Gutierrez; Eric M Ferreira
Journal:  J Am Chem Soc       Date:  2010-07-07       Impact factor: 15.419

2.  Au-Catalyzed Intermolecular [2+2] Cycloadditions between Chloroalkynes and Unactivated Alkenes.

Authors:  Yu-Bin Bai; Zaigang Luo; Yuguang Wang; Jin-Ming Gao; Liming Zhang
Journal:  J Am Chem Soc       Date:  2018-04-17       Impact factor: 15.419

  2 in total

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