Literature DB >> 15007403

Stereoselective preparation of conjugated E-enynes from E-vinylic tellurides and terminal alkynes via Sonogashira cross-coupling.

Gilson Zeni1, Diego Alves, Jesus M Pena, Antonio L Braga, Helio A Stefani, Cristina W Nogueira.   

Abstract

E-Vinylic tellurides undergo a direct cross-coupling reaction with terminal alkynes in the presence of palladium(II)/CuI in Et(3)N at room temperature to give E-enynes in good yields. The methodology represents a general and efficient protocol for carrying out the synthesis of E-enynes under mild conditions with complete retention of configuration.

Entities:  

Year:  2004        PMID: 15007403     DOI: 10.1039/b401059k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Efficient Protocol for Synthesis of β-Hydroxy(alkoxy)selenides via Electrochemical Iodide-Catalyzed Oxyselenation of Styrene Derivatives with Dialkyl(aryl)diselenides.

Authors:  Jinyang Chen; Lan Mei; Haiying Wang; Li Hu; Xiaorui Sun; Jianwei Shi; Qiang Li
Journal:  ChemistryOpen       Date:  2019-09-10       Impact factor: 2.911

  1 in total

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