KF/Al2O3as a Highly Efficient, Green, Heterogeneous, and Reusable Catalytic System for the Solvent-Free Synthesis of Carboacyclic Nucleosides via Michael Addition Reaction-Reference-Cited by-同舟云学术

KF/Al2O3as a Highly Efficient, Green, Heterogeneous, and Reusable Catalytic System for the Solvent-Free Synthesis of Carboacyclic Nucleosides via Michael Addition Reaction

Published:2008-12-16 Issue:1 Volume:39 Page:139-157
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Zare Abdolkarim,Hasaninejad Alireza,Beyzavi Mohammad Hassan,Zare Ahmad Reza Moosavi,Khalafi-Nezhad Ali,Asadi Fatemeh,Baramaki Leila,Jomhori-Angali Sedigheh,Ghaleh-Golabi Rokhsareh

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397910802369711

Reference6 articles.

1. KF–Al 2 O 3 is an efficient solid support reagent for the acetylation of amines, alcohols, and phenols. Impeding effect of solvent on the reaction rate

2. Zinc oxide-tetrabutylammonium bromide tandem as a highly efficient, green, and reusable catalyst for the Michael addition of pyrimidine and purine nucleobases to α,β-unsaturated esters under solvent-free conditions

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